3003 90 000 0 — Medicaments (excluding goods of heading 3002, 3005 or 3006) consisting of two or more constituents which have been mixed together for therapeutic or prophylactic uses, not put up in measured doses or in forms or packings for retail sale: other
Medicaments (excluding goods of heading 3002, 3005 or 3006) consisting of two or more constituents which have been mixed together for therapeutic or prophylactic uses, not put up in measured doses or in forms or packings for retail sale: other
Names come in English where the EU Combined Nomenclature publishes them — chapters, headings and subheadings, whose first six digits are the same Harmonized System; deeper EAEU detail is a machine translation, marked as such. Official texts — tariff notes, measures, lists and classification rulings — are the original: customs and your broker go by that wording. Where we show a machine translation of them, it is marked; where our quality check rejected one, the Russian stays.
Machine translation. The original is the Russian text of the EAEU tariff, and customs goes by it; this translation is for understanding only and has no legal force.
This is the base rate. A tariff quota, a preference for the country of origin and a tariff exemption lower it; anti-dumping and special duties are paid on top of it
EEC Council Decision No. 80 of 14.09.2021
- Veterinary, plant quarantine and sanitary control2
- Mandatory labelling1
- Conformity assessment1
- EAEU non-tariff regulation1
None: russian bans and restrictions, recycling fee, export control, trade defence measures — duty on top of the tariff, tariff quota.
Whether a measure applies to your goods depends on their characteristics and the shipping documents
The general import rate in Russia: Tax Code of Russia, Art. 164(3) (Federal Law No. 425-FZ of 28.11.2025). This code is not named on the 10% VAT list (Decree No. 908) or the exemption list (No. 1042). The list of medical goods No. 688 is not checked here.
Product reference in Word (in Russian)
Duties, taxes, fees, bans, permits and controls in one free file.
Import into Russia
Import referenceExport from Russia
Export referenceImport into Russia
Payments on import
Duty for this code: 0%. On top of the duty, on import into Russia you pay VAT of 22% of the customs value including the duty (Article 160 of the Tax Code) and the customs processing fee — a fixed amount by value band. Customs value: the price of the goods, delivery to the border, local costs.
CCT rate: the EAEU CCT as amended by Решение Совета ЕЭК № 80 от 14.09.2021, from 01.01.2022; our register has no later decisions on the rate for this code.
Customs fee scale by customs value, 2026
- from 0 to 200,000 ₽1,231 ₽
- from 200,000 to 450,000 ₽2,462 ₽
- from 450,000 to 1,200,000 ₽4,924 ₽
- from 1,200,000 to 2,700,000 ₽13,541 ₽
- from 2,700,000 to 4,200,000 ₽18,465 ₽
- from 4,200,000 to 5,500,000 ₽21,344 ₽
- from 5,500,000 to 10,000,000 ₽49,240 ₽
- over 10,000,000 ₽73,860 ₽
Fee per declaration. Russian Government Resolution No. 1637 of 28.11.2024 as amended by Resolution No. 1638 of 23.10.2025.
Import VAT in EAEU countries
- Russia22%Tax Code of Russia, Art. 164(3) (Federal Law No. 425-FZ of 28.11.2025)
- Kazakhstan16%Tax Code of Kazakhstan, Art. 503(1), from 01.01.2026
- Belarus20%Tax Code of Belarus, Art. 122
- Armenia20%Tax Code of the Republic of Armenia
- Kyrgyzstan12%Tax Code of the Kyrgyz Republic
Standard rate; each country has reduced rates and exemptions for some goods. The duty for the code above is the union one, the same for all
Customs declaration fee
- Kazakhstan6 MCI per goods declaration, KZT 25,950 in 2026
- BelarusBYN 50 for goods of chapter 30from Jan 1, 2027: BYN 55
- ArmeniaAMD 3,500 for clearanceinspection and recording: AMD 1,000 per consignment up to 1 t and AMD 300 per each additional tonne
- Kyrgyzstan0.4% of the customs valuenot less than 5 and not more than 2,500 calculation units
Tariff preferences
The code is on the EAEU list of preferential goods: for goods originating in a beneficiary country the duty is lower
33 countries
Algeria, Egypt, Venezuela, São Tomé & Príncipe, Sri Lanka, Jordan, Iran, Pakistan, North Korea, Bhutan, Morocco, Eswatini, Lebanon, Bolivia, Mongolia, Papua New Guinea, Samoa, Vanuatu, Ghana, Honduras, Zimbabwe, Cape Verde, Cameroon, Kenya, Congo - Brazzaville, Côte d’Ivoire, Cuba, Namibia, Nicaragua, Philippines, Tunisia, Nigeria, Micronesia
46 countries
Burkina Faso, Guinea, Eritrea, Congo - Kinshasa, Timor-Leste, Afghanistan, Mauritania, Yemen, Cambodia, Lesotho, Laos, Bangladesh, Nepal, Tanzania, Palestinian Territories, Angola, Benin, Burundi, Haiti, Gambia, Guinea-Bissau, Djibouti, Zambia, Kiribati, Liberia, Madagascar, Malawi, Mali, Mozambique, Niger, Rwanda, Senegal, Myanmar (Burma), Sudan, Sierra Leone, Uganda, Chad, South Sudan, Syria, Solomon Islands, Comoros, Togo, Tuvalu, Ethiopia, Somalia, Central African Republic
The preference requires a document of origin and compliance with the direct consignment rule; customs checks the right to it at declaration.
Documents required
A summary across all the lists we check: the document, its legal basis and whether it covers the whole code. Details are in the sections below.
- Declaration of conformityПостановление № 2425 · covers part of the goods under the code
- Declaration based on the applicant's own evidence (instead of a certificate)Постановление Правительства РФ № 353, приложение № 18, пункт 6 · until 01.09.2027 per batch; applicant: a Russian company or sole trader; valid for 6 months, no EAC mark
- Sanitary and epidemiological controlРешение Коллегии Евразийской экономической комиссии от 17.09.2019 № 154 · covers part of the goods under the code
- Veterinary certificateРешение Коллегии Евразийской экономической комиссии от 20.01.2020 № 13 · covers part of the goods under the code
- Licence or permitРешение Коллегии ЕЭК № 30, раздел 2.12
- Mandatory identification markingРаспоряжение № 792-р, пункт 77
- Medicine registration and markingФедеральный закон № 61-ФЗ, статьи 47 и 67 · if the product is of this type
Goods in customs transit may be tracked with a navigation seal: this depends on the route and procedure, not on the code (EAEU Agreement of 19.04.2022, EEC Board Decision No. 84).
Customs declaration hints
Boxes 33, 36, 44, 47
Customs declaration hints
Boxes 33, 36, 44, 47
Which codes go into the boxes of the goods declaration for this product. The codes come from the classifiers of Customs Union Commission Decision No. 378. Reliefs, document types and excise depend on the shipment, so such lines carry a condition.
Box 33 · Commodity code
- 3003900000
- Сin the second subdivision, if the goods do not fall under the bans and restrictions that apply to the code
- Мin the second subdivision, if the goods are on the marking list but its requirements do not apply to them
- Оin the second subdivision, if goods with different names are declared under one code
Box 36 · Preference
- ОООО-ООFees, duty, excise, VAT: no relief claimed, no excise (dash)
- ООГГ-ООТарифная преференция в отношении товаров, происходящих из развивающихся стран · if the goods originate in a developing country and origin is proven
- ООНН-ООТарифная преференция в отношении товаров, происходящих из наименее развитых стран · if the goods originate in a least developed country and origin is proven
Box 44 · Documents produced
- 01408Документ об оценке соответствия, предусмотренный законодательством государства – члена Евразийского экономического союза, на территории которого продукция (товар) помещается под таможенные процедуры · Постановление № 2425
- 01201Ветеринарный сертификат · Решение Коллегии Евразийской экономической комиссии от 20.01.2020 № 13
- 01011Лицензия на экспорт и (или) импорт товаров · Решение Коллегии ЕЭК № 30, раздел 2.12
- 06013Сертификат о происхождении товара формы "А" · if the goods are imported under a tariff preference
Box 47 · Calculation of payments
- 1010Таможенные сборы за совершение таможенных операций (за таможенное оформление товаров, за таможенное декларирование товаров, за таможенные операции)
- 2010Ввозная таможенная пошлина (иные пошлины, налоги и сборы, имеющие эквивалентное действие), обязанность по уплате которой возникла с 1 сентября 2010 г.
- 5010Налог на добавленную стоимость
Completion rules and classifiers: Решение Комиссии Таможенного союза от 20.05.2010 № 257; классификаторы — Решение Комиссии Таможенного союза от 20.09.2010 № 378
Each requirement in detailMedicinal products · Mandatory labelling · Veterinary, plant quarantine and sanitary control · Conformity assessment · How it is certified · EAEU non-tariff regulation
Medicinal products
If the product is a medicinal product for human use, only registered products may be imported (Article 47 of Federal Law No. 61-FZ), they are marked with identification codes (Article 67 of the same law, Government Resolution No. 1556), and import VAT is 10% under the code list of Government Resolution No. 688.
Mandatory labelling
The code is named in the list of goods subject to labelling with identification means. Whether your product must be labelled depends on its name and its OKPD 2 code.
Item 77. Лекарственные препараты для ветеринарного применения
Labelling mandatory from: 1 сентября 2024 г.; 1 марта 2026 г.
Russian Government Order No. 792-r of 28.04.2018 as amended by Orders No. 1765-r of 04.07.2024, No. 249-r of 07.02.2025 and No. 956-r of 27.04.2026. Deadlines and procedures for individual groups are set by Government resolutions on labelling rules.
Veterinary, plant quarantine and sanitary control
Goods fall under supervision by their type and characteristics
Sanitary and epidemiological supervision (control)
rule for the whole chapter 30Материалы для изделий (изделия), контактирующих с кожей человека, одежда, обувь; Иная продукция (товары), в отношении которой одним из государств – членов Евразийского экономического союза введены временные санитарные мерыThe list names this code with “ex”: control applies only to goods with this description.
Решение Коллегии Евразийской экономической комиссии от 17.09.2019 № 154
Veterinary control (supervision)
rule for the whole chapter 30Фармацевтическая продукция (для применения в ветеринарии)The list names this code with “ex”: control applies only to goods with this description.
Such goods need a veterinary certificate, and the manufacturing plant must be on the register of third-country establishments. Check the supplier in the register →
Решение Коллегии Евразийской экономической комиссии от 20.01.2020 № 13
Conformity assessment
May applyWhether the goods fall under a regulation depends on their name and characteristics. Check them against the list
- Постановление № 2425Единый перечень продукции: сертификация и декларирование в РФ
- Кормогризин — declaration of conformity (part of the heading) · ГОСТ Р 57244-2016, ГОСТ 13496.13-2018, ГОСТ 10199-2017
С 1 сентября 2022 г. декларация о соответствии такой продукции принимается при наличии у изготовителя (продавца) протокола исследований (испытаний) и измерений, проведенных аккредитованной в национальной системе аккредитации испытательной лабораторией (центром).
Checked: the consolidated list of Government Decree No. 2425 and the lists of 42 technical regulations out of 52 adopted. The others have no list by HS code, so see the full list of regulations.
How it is certified
Valid documents in the EAEU unified register for subheading 3003 90: certificates 0, declarations 4.
- By technical regulation
- ТР ТС 029/20122ТР ТС 021/20112ТР ТС 022/20112ТР ТС 009/20112
- Schemes
- 3д4The letter after the scheme number shows the form: certification or declaration of conformity.
- Manufacturers outside the EAEU
- India2Thailand1
Manufacturers of these goods →Check a supplier’s document by its number →
EAEU non-tariff regulation
Unified list of non-tariff measures (EEC Board Decision No. 30 of 21.04.2015). List entries selected by code
- 2.12licensing regimeon import and export
Наркотические средства, психотропные вещества и их прекурсоры
5 list entriesОксикодон текодин 14-гидроксидигидрокодеинон; алкалоидов опия в; свернувшийся сок опийного или; Апрофен тарен 7-[(10,11-дигидро-5H-дибензо[a,d]; (+)-альфа-метилфенэтиламин 170. Декстрометорфан
Export from Russia
Documents required
A summary across all the lists we check: the document, its legal basis and whether it covers the whole code. Details are in the sections below.
- Licence or permitРешение Коллегии ЕЭК № 30, раздел 2.12
- Veterinary certificateВетеринарные требования страны ввоза · if the importing country requires it · covers part of the goods under the code
Customs declaration hints
Boxes 33, 44, 47
Customs declaration hints
Boxes 33, 44, 47
Which codes go into the boxes of the goods declaration for this product. The codes come from the classifiers of Customs Union Commission Decision No. 378. Reliefs, document types and excise depend on the shipment, so such lines carry a condition.
Box 33 · Commodity code
- 3003900000
- Оin the second subdivision, if goods with different names are declared under one code
Box 44 · Documents produced
- 01011Лицензия на экспорт и (или) импорт товаров · Решение Коллегии ЕЭК № 30, раздел 2.12
- 01201Ветеринарный сертификат · Ветеринарные требования страны ввоза
Box 47 · Calculation of payments
- 1010Таможенные сборы за совершение таможенных операций (за таможенное оформление товаров, за таможенное декларирование товаров, за таможенные операции)
Completion rules and classifiers: Решение Комиссии Таможенного союза от 20.05.2010 № 257; классификаторы — Решение Комиссии Таможенного союза от 20.09.2010 № 378
Classification
Where it sits in the nomenclature
Section VI. Products of the chemical or allied industries
- 30Pharmaceutical products
- 3003Medicaments consisting of two or more constituents mixed together for therapeutic or prophylactic uses, not in measured doses or put up for retail sale (excl. goods of heading 3002, 3005 or 3006)
- 3003 90Medicaments consisting of two or more constituents mixed together for therapeutic or prophylactic uses, not in measured doses or put up for retail sale (excl. antibiotics containing hormones or steroids used as hormones, but not containing antibiotics, alkaloids or derivatives thereof, hormones, antibiotics, antimalarial active principles or goods of heading 3002, 3005 or 3006)
- 3003 90 00Other
- 3003 90 000 0you are here
Explanatory notes to heading 3003 4 paragraphs
Machine translation from Russian. The original is the EEC explanatory note, and that is what a classification dispute is argued from; the translation is for understanding and has no legal force.
3003 Medicaments (excluding goods of heading 3002, 3005 or 3006) consisting of two or more constituents which have been mixed together for therapeutic or prophylactic uses, not put up in measured doses or in forms or packings for retail sale: 3003 10 – containing penicillins or derivatives thereof, with a penicillanic acid structure, or streptomycins or their derivatives 3003 20 – other, containing antibiotics – other, containing hormones or other products of heading 2937: 3003 31 – – containing insulin 3003 39 – – other – other, containing alkaloids or derivatives thereof: 3003 41 – – containing ephedrine or its salts 3003 42 – – containing pseudoephedrine (INN) or its salts 3003 43 – – containing norephedrine or its salts 3003 49 – – other 3003 60 – other, containing antimalarial active principles described in Subheading Note 2 to this Chapter 3003 90 – other
This heading covers medicinal products used for internal or external use or for the prevention of human or animal diseases. Such means are obtained by mixing two or more components. However, packaged in dosage form or in retail packages, they are classified in heading 3004. This heading includes: (1) Mixed medicaments, such as preparations listed in official pharmacopoeias, proprietary preparations, etc., including preparations manufactured in the form of throat and mouth rinses, eye drops, ointments, liniments, injectable solutions, anti-inflammatory and other preparations, not included in heading 3002, 3005 or 3006. However, it is not to be understood that preparations registered in official pharmacopoeias, proprietary preparations, etc. are always classified in heading 3003. For example, acne preparations intended primarily for skin cleansing and not containing sufficiently high concentrations of active ingredients to be considered as having primary therapeutic or prophylactic effect against acne are to be classified in heading 3304. (2) Preparations containing one active substance in a mixture with a filler, sweetener, agglomerating substance, carrier, etc. (3) Drugs intended for nutrition, administered exclusively intravenously, for example, by intravenous infusion through a syringe or dropper. (4) Colloidal solutions and suspensions (for example, colloidal selenium) for medical purposes, except for colloidal sulfur or precious metals in the colloidal state.
Colloidal sulphur is classified in heading 3004 when packaged as dosage forms or in retail packages for therapeutic or prophylactic use and in heading 2802 in all other cases. Precious metals in the colloidal state are classified in heading 2843, whether they are used in sludge or not for medical purposes. Mixtures of precious metals in a colloidal state or mixtures of one or more precious metals in a colloidal state with other substances used for therapeutic or prophylactic purposes are, however, classified in this heading. (5) Medicinal complex plant extracts, including extracts obtained by processing plant mixtures. (6) Medicinal mixtures of plants or plant parts of heading 1211. (7) Therapeutic salts obtained by evaporation of natural m ineral waters, and similar products obtained artificially. (8) Concentrated water of salt sources (e.g. Kreutsnach water) used in therapy; mixtures of salts prepared for therapeutic baths (sulphur, iodine, etc. baths), without the addition or with the addition of aromatic substances. (9) Therapeutic salts (for example, a mixture of sodium bicarbonate, tartaric acid, magnesium sulfate and sugar) and similar mixed gas-emitting salts used for medical purposes. (10) Camphor oil, phenolic oil, etc. (11) Anti-asthmatic products such as anti-asthmatic paper and powders. (12) "Long-acting drugs", such as preparations in which the drug component is fixed on a polymeric ion exchange material. (13) Anesthetics used in medicine, veterinary medicine or surgery. The provisions of this heading do not apply to foodstuffs or beverages such as dietary, diabetic or nutritionally fortified foodstuffs, tonic beverages or minerals in odes (natural or artificial) which fall under the relevant headings. This is usually the case with dietary supplements containing only nutrients. The main nutrients in foods are proteins, carbon levodes and fats. Vitamins and mineral salts also play a role in nutrition. Similarly, foodstuffs and beverages containing medicinal substances are not included in this heading if these substances are added for the sole purpose of improving the dietary balance, increasing the energy content or nutritional value of the product or improving its taste and aromatic qualities, provided that the product retains its properties as a food or beverage. In addition, products consisting of a mixture of plants or parts of plants, or consisting of plants and parts of plants mixed with other substances, used for the preparation of herbal infusions or herbal “teas” (for example, herbal infusions or herbal “teas” having laxatives, cleansing, diuretics or wind-burning properties), and which are said to alleviate malaise or favorably affect general health and well-being, are also excluded from this heading (heading 2106). In addition, this heading does not include food additives containing vitamins or mineral salts which are prepared for the purpose of promoting health and improving well-being, but have no instructions for their use for the prevention or treatment of diseases or ailments. Such products, usually manufactured in liquid form but which may also be supplied in powders or tablets, are generally classified in heading 2106 or Chapter 22.
However, this heading covers preparations in which a food product or drink merely serves as a carrier, filler or sweetener for medicinal substances (for example, to improve digestion). In addition to foodstuffs and beverages, this heading does not include: (a) goods of heading 3002, 3005 or 3006; (b) aqueous distillates or aqueous solutions of essential oils and goods of headings 3303 to 3307, even if they have therapeutic or prophylactic properties (Chapter 33); (c) soaps containing medicinal products (heading 3401); (d) insecticides, disinfectants, etc. of heading 3808.
Official text adopted by a Recommendation of the EEC Board
Notes to chapter 30 — Pharmaceutical products 6 items
Notes
Machine translation. The original is the Russian text of the EAEU tariff, and customs goes by it; this translation is for understanding only and has no legal force.
1. This group does not include:
(a) food or beverages (such as dietary, diabetic or nutritionally fortified foods, food additives, tonic beverages and mineral waters), other than nutrient preparations for intravenous administration (Section IV);
(b) products such as tablets, chewing gum or patches (transdermal systems) containing nicotine and intended to contribute to the cessation of tobacco consumption (heading 2404);
(c) specially calcified or finely ground plasters for use in dentistry (heading 2520);
(d) aqueous distillates or aqueous solutions of essential oils intended for medical use (heading 3301);
(e) preparations of headings 3303 to 3307, even if they have therapeutic or prophylactic properties;
(f) soap or other products of heading 3401 containing medicinal additives;
(g) g gypsum-based products for use in dentistry (heading 3407);
(h) blood albumin not prepared for therapeutic or prophylactic use (heading 3502); or
(ij) diagnostic reagents of heading 3822.
2. For the purposes of heading 3002, the term “immunological products” applies to peptides and proteins (other than those of heading 2937) which are directly involved in the regulation of immunological processes such as monoclonal antibodies (MABs), antibody fragments, antibody conjugates and antibody fragment conjugates, interleukins, interferons (IFNs), chemokines and certain tumor necrosis factors (TNFs), growth factors (GFs), hematopoietines and colony-stimulating factors (CSFs).
3. In headings 3003 and 3004 and note 4(d) to this chapter it is understood:
(a) unmixed products:
(1) unmixed products dissolved in water;
(2) all goods of Chapter 28 or 29; and
(3) simple plant extracts of heading 1302, only standardized or dissolved in any solvent;
(b) under mixed products:
(1) colloidal solutions and suspensions (except colloidal sulfur);
(2) plant extracts obtained by treatment of mixtures of plant raw materials; and
(3) salts and concentrates obtained by evaporation of natural mineral waters.
4. Heading 3006 covers only the following products, which are to be classified in this and no other heading of the Nomenclature:
(a) sterile surgical ketgut, similar sterile suture materials (including sterile absorbable surgical or dental threads) and sterile adhesive tissues for surgical wound closure;
(b) sterile kelp and sterile tampons of kelp;
(c) sterile resorbable surgical or dental hemostatic agents (hemostatics); sterile surgical or dental adhesive barriers, resorbable or non-absorbable;
(d) contrast preparations for X-ray examinations and diagnostic reagents intended for administration to patients, which are unmixed substances in dosage forms or substances consisting of two or more components mixed for such use;
(e) placebos and sets of impersonal clinical preparations for the conduct of approved clinical trials by simple blind (or double blind) method, packaged in dosage forms, even if they may contain active (active) medicinal substances;
(f) dental cements and other materials for filling teeth; cements for reconstructing bone;
(g) sanitary bags and first aid kits;
(h) chemical contraceptives based on hormones, other compounds of heading 2937 or spermicides;
(ij) preparations in the form of a gel intended for use in medicine or veterinary medicine as a lubricant for body parts in surgical operations or physical investigations or as a binding agent between the body and medical instruments;
(k) unsuitable pharmaceuticals, i.e. pharmaceutical products, which are not suitable for use for their original purpose, for example because they have expired; and
(l) devices identified as devices for stomic use, i.e. colostomy, ileostomy and urostomy bags cut in shape and their sticky plates or front parts.
Subheading notes
English text as published in Annex I to Regulation (EU) 2021/1832 (Combined Nomenclature). The EAEU tariff and the EU nomenclature copy these notes from the same convention. For a Russian declaration the binding version is the Russian one: Annex to Decision No 80 of the EEC Council of 14 September 2021.
1. For the purposes of subheadings 3002 13 and 3002 14, the following are to be treated:
(a) as unmixed products, pure products, whether or not containing impurities;
(b) as products which have been mixed:
(1) the products mentioned in (a) above dissolved in water or in other solvents;
(2) the products mentioned in (a) and (b) (1) above with an added stabiliser necessary for their preservation or transport; and
(3) The products mentioned in (a), (b) (1) and (b) (2) above with any other additive.
2. Subheadings 3003 60 and 3004 60 cover medicaments containing artemisinin (INN) for oral ingestion combined with other pharmaceutical active ingredients, or containing any of the following active principles, whether or not combined with other pharmaceutical active ingredients : amodiaquine (INN); artelinic acid or its salts; artenimol (INN); artemotil (INN); artemether (INN); artesunate (INN); chloroquine (INN); dihydroartemisinin (INN); lumefantrine (INN); mefloquine (INN); piperaquine (INN); pyrimethamine (INN) or sulfadoxine (INN).
Classification rulings for this code (2)
Machine translation from Russian. The original is the Russian wording of the ruling, and customs goes by it; this translation is for understanding only and has no legal force.
Omeprazole pellets 8.5% is a pharmaceutical substance - spherical pellets from white to almost white. containing the active ingredient omeprazole pellets (including omeprazole 20 mg) 235 mg, [omeprazole 8.5%, auxiliary substances - sodium hydrophosphate (sodium phosphate bisubstituted), sodium lauryl sulfate, lactose monohydrate, cornstarch, Mannitol, sucrose, sucrose (Sugar Regular), Hypromellose (hydroxypropylmethylcellulose), propylene glycol, sodium hydroxide, cetyl alcohol, methacrylic acid and etacrylate copolymer [1:1], polysorbate-80, Titanium dioxide.
Full descriptionCollapse description
Used in the production of a drug for the treatment of acid-dependent diseases capsules intestinal, by filling each capsule with a pharmaceutical substance. The pharmaceutical substance omeprazole pellets is supplied in a mound in plastic drums with an internal plastic bag.
GRI 1 and 6
Фармацевтическая субстанция-раствор » в виде прозрачной, вязкой жидкости от бесцветной до светло-желтого с коричневатым оттенком цвета, содержащая в 1 л в качестве действующего вещества - лактулозу 667,0 г, в качестве вспомогательного вещества - воду очищенную до 1000 мл, применяется в качестве слабительного средства.
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Поставляется наливом в автоцистерне в количестве 17 820 л для последующего розлива (без дополнительной обработки) во флаконы объемом 200, 500 и 1000 мл для розничной продажи как лекарственный препарат [наименование опущено].
GRI 1 and 6
Rulings of other EAEU countries for this code (6)
An advance ruling binds only the country that issued it, but it shows how neighbours in the Union classify this product.
The EEC publishes these rulings in Russian only, and they are shown as published.
Belarus
Недозированное лекарственное средство в форме белых или почти белых микропеллет, применяемое при артериальной гипертензии, стенокардии, хронической сердечной недостаточности, нарушениях сердечного ритма, функциональных нарушениях сердечной деятельности, профилактике приступов мигрени.
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Состав: метопролола сукцинат (действующее вещество) – 60,0%, сферы микрокристаллической целлюлозы (матрица) – 21,2%, кремния диоксид коллоидный безводный (лубрикант) – 1,0%, гипромеллоза (HPMC E5) (связующее вещество) – 0,3%, сахароза (наполнитель) – 2,5%, этилцеллюлоза (N-50) (вещество для пролонгации действия действующего вещества) – 11,7%, стеариновая кислота (лубрикант) – 2,2%, полиэтиленгликоль (6000) (связующее вещество) – 1,1%. Используется для производства лекарственного средства в капсулах «МЕТОПРОЛОЛ-ЛФ 100мг»: микропеллеты засыпаются в капсулирующую машину, которая дозирует нужное количество вещества (микропеллет) в капсулы, затем готовые капсулы расфасовываются по блистерам и упаковываются в коробки для розничной продажи.
Товар поставляется в бочках по 1-50 кг, снабженных этикеткой, содержащей сведения о наименовании товара, его производителе, дате производства, условиях хранения и транспортировки, др. информацию.
В соответствии с ОПИ 1, 5(б) и 6 единой ТН ВЭД ЕАЭС, пояснения к товарной позиции 3003
Belarus
Недозированное лекарственное средство в форме белых или почти белых сферических пеллет размером от 0,71 мм до 1,00 мм.
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Состав: тамсулозина гидрохлорид - 0,20% (действующее вещество), сахарные гранулы - 93,38% (наполнитель), лекарственное покрытие для защиты от желудочного сока L 100 - 4,00 %, макрогол 6000 - 0,74% (наполнитель), этилцеллюлоза - 1,67% (наполнитель), изопропиловый спирт и вода в качестве увлажнителя. Используется при производстве лекарственного средства в капсулах «Тамсулозин 0,2мг, 0,4мг». Пеллеты засыпаются в капсулирующую машину, где происходит дозировка вещества (пеллет) в капсулы, затем капсулы запаковываются в блистеры и упаковку для розничной продажи.
Поставляется в бочках 1-50 кг. Бочки снабжены этикеткой, на которой указана следующая информация: наименование товара, производитель, номер серии, дата производства, срок годности, вес нетто, вес брутто, условия хранения и транспортировки товара.
В соответствии с ОПИ 1, 5б и 6, пояснения к товарной позиции 3003
Belarus
Недозированное лекарственное средство в форме пеллет, применяемое для лечения ожирения.
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Состав пеллет: орлистат (действующее вещество) – 50%, гидроксипропилметилцеллюлоза (наполнитель) – 44%, натрия лаурилсульфат (дезинтегрант) – 4%, натрия крахмалгликолят (дезинтегрант) – 2%. Используется для производства лекарственного средства в капсулах «Фигурин 60мг»: пеллеты засыпаются в капсулирующую машину, которая дозирует нужное количество вещества (пеллет) в капсулы, затем готовые капсулы расфасовываются по блистерам и упаковываются в коробки для розничной продажи.
Товар поставляется в бочках по 1-50 кг, снабженных этикеткой, содержащей сведения о наименовании товара, его производителе, дате производства, весе, др. информацию.
В соответствии с ОПИ 1, 5(б) и 6, пояснения к товарной позиции 3003
The right code is in the HS code search.