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The tariff classification of ACTIMMUNE® (Interferon gamma-1b), imported put up in single-dose vials for subcutaneous injection, from Austria and Germany
Issued January 4, 2002 by U.S. Customs and Border Protection.
Cite this ruling
Copies to clipboardH8 H86293 (January 4, 2002)
Tariff classification
HTS codes: 3004.90.9190
Headings: 3004
Product description
The subject product, ACTIMMUNE® (Interferon gamma-1b), is a medicament containing Interferon gamma-1b (an analog of human interferon gamma, produced by recombinant DNA technology) as the active ingredient. ACTIMMUNE® is indicated for use in the treatment of chronic granulomatous disease and severe, malignant osteopetrosis.
CBP rationale
The applicable subheading for the subject product will be 3004.90.9190, Harmonized Tariff Schedule of the United States (HTS), which provides for Medicaments … consisiting 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: Other.
Full text
NY H86293 January 4, 2002 CLA-2-30:RR:NC:2:238 H86293 CATEGORY: Classification TARIFF NO.: 3004.90.9190 Matthew T. McGrath, Esq. Barnes, Richardson & Colburn 1225 Eye Street, N.W. Suite 1150 Washington, DC 20005 RE: The tariff classification of ACTIMMUNE® (Interferon gamma-1b), imported put up in single-dose vials for subcutaneous injection, from Austria and Germany Dear Mr. McGrath: In your letter dated December 12, 2001, on behalf of your client, InterMune, Inc. you requested a tariff classification ruling. The subject product, ACTIMMUNE® (Interferon gamma-1b), is a medicament containing Interferon gamma-1b (an analog of human interferon gamma, produced by recombinant DNA technology) as the active ingredient. ACTIMMUNE® is indicated for use in the treatment of chronic granulomatous disease and severe, malignant osteopetrosis. The applicable subheading for the subject product will be 3004.90.9190, Harmonized Tariff Schedule of the United States (HTS), which provides for Medicaments … consisiting 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: Other. The rate of duty will be free. This merchandise may be subject to the requirements of the Federal Food, Drug, and Cosmetic Act, which is administered by the U.S. Food and Drug Administration. You may contact them at 5600 Fishers Lane, Rockville, Maryland 20857, telephone number 301-443-1544. 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 Harvey Kuperstein at 646-733-3033. Sincerely, Robert B. Swierupski Director, National Commodity Specialist Division
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