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The tariff classification of Ambrisentan Tablets in dosage form, from India
Issued July 16, 2018 by U.S. Customs and Border Protection.
Cite this ruling
Copies to clipboardN2 N298542 (July 16, 2018)
Tariff classification
HTS codes: 3004.90.9220
Headings: 3004
Product description
Ambrisentan is an orally active selective type A endothelin receptor antagonist (ERA) indicated for the treatment of pulmonary arterial hypertension (PAH). It will be imported in dosage form in 5 mg and 10 mg tablets.
CBP rationale
The applicable subheading for the Ambrisentan Tablets in dosage form will be 3004.90.9220, Harmonized Tariff Schedule of the United States (HTSUS), which provides for “Medicaments … consisting of mixed or unmixed products for therapeutic or prophylactic uses, put up in measured doses … or in forms or packings for retail sale: Other: Other: Other: Cardiovascular medicaments.
Full text
N298542 July 16, 2018 CLA-2-30:OT:RR:NC:N1:138 CATEGORY: Classification TARIFF NO.: 3004.90.9220 Mr. Pradeep Shah Zydus Pharmaceuticals USA, Inc. 73 Route 31 North Pennington, NJ 08534 RE: The tariff classification of Ambrisentan Tablets in dosage form, from India Dear Mr. Shah: In your letter dated June 18, 2018, you requested a tariff classification ruling. Ambrisentan is an orally active selective type A endothelin receptor antagonist (ERA) indicated for the treatment of pulmonary arterial hypertension (PAH). It will be imported in dosage form in 5 mg and 10 mg tablets. The applicable subheading for the Ambrisentan Tablets in dosage form will be 3004.90.9220, Harmonized Tariff Schedule of the United States (HTSUS), which provides for “Medicaments … consisting of mixed or unmixed products for therapeutic or prophylactic uses, put up in measured doses … or in forms or packings for retail sale: Other: Other: Other: Cardiovascular medicaments.” The rate of duty will be free. Duty rates are provided for your convenience and are subject to change. The text of the most recent HTSUS and the accompanying duty rates are provided on the World Wide Web at https://hts.usitc.gov/current. This merchandise may be subject to the Federal Food, Drug, and Cosmetic Act and/or The Public Health Security and Bioterrorism Preparedness and Response Act of 2002 (The Bioterrorism Act), which are administered by the U.S. Food and Drug Administration (FDA). Information on the Federal Food, Drug, and Cosmetic Act, as well as The Bioterrorism Act, can be obtained by calling the FDA at 1-888-463-6332, or by visiting their website at www.fda.gov. This ruling is being issued under the provisions of Part 177 of the Customs Regulations (19 C.F.R. 177). A copy of the ruling or the control number indicated above should be provided with the entry documents filed at the time this merchandise is imported. If you have any questions regarding the ruling, contact National Import Specialist Judy Lee at [email protected]. Sincerely, Steven A. Mack Director National Commodity Specialist Division
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