Medicaments (excluding goods of heading 3002, 3005 or 3006) consisting of mixed or unmixed products for therapeutic or prophylactic uses, put up in measured doses (including those in the form of transdermal administration systems) or in forms or packings for retail sale:
Part of: 30 — Pharmaceutical products
N347734 · 2025-05-08 — The tariff classification of Peritoneal Dialysis (PD) solutions of Extraneal® (icodextrin) and Dianeal® (dextrose), in dosage form, from Mexico
We note that the request did not seek a determination as to country of origin, or as to the applicability of preferential treatment under the U.S.-Mexico-Canada Agreement; as such, this ruling does not address those issues. The Peritoneal Dialysis (PD) solutions imported in ultrabags are used to remove excess fluid, correct electrolyte problems, and remove toxins in those with kidney failure. Extraneal (icodextrin) is indicated for the management of kidney failure in patients requiring long-term kidney replacement therapy. Dianeal (dextrose) is indicated for the management of acute or chronic…
H312361 · 2023-08-21 — Revocation of NY N276739 and HQ 957022; Classification of sodium bicarbonate cartridges/bags
This is in reference to New York Ruling Letter (NY) N276739, issued to you by U.S. Customs and Border Protection (CBP) on July 12, 2016, concerning classification of a “Bibag” from France, under the Harmonized Tariff Schedule of the United States (HTSUS). We have reviewed that decision, and determined that it is incorrect, and for the reasons set forth below, are revoking your ruling. We have also reviewed Headquarters Ruling (HQ) 957022, dated January 24, 1995, and for similar reasons set forth below, are revoking that ruling. Pursuant to section 625(c)(1), Tariff Act of 1930 (19 U.S.C.…
H304287 · 2019-10-29 — Tariff classification of Sevoflurane packaged in 250 ml bottles
for a binding ruling regarding the tariff classification of Sevoflurane under the Harmonized Tariff Schedule of the United States (HTSUS). FACTS: Sevoflurane is an inhalation anesthesia. It is manufactured from Hexafluroisopropyl Methyl Ether sourced from India and/or China. It is packaged in bottles of 250 ml which are sold to pharmaceutical distributors in boxes of six. You state that Sevoflurane from a single 250 ml bottle may be used for one or more patients by the anesthesiologist, based on the particular patient. The sample label on the 250 ml bottle that you provided and package insert…
N282730 · 2017-02-21 — The tariff classification of Glatiramer Acetate (CAS No. 147245-92-9) in bulk form and Glatiramer Acetate injection in dosage form, from India
Glatiramer Acetate will be imported in bulk form and in 20mg/mL and 40mg/mL single dose pre-filled syringes. Glatiramer Acetate is an immunomodulator drug that is indicated for the treatment of patients with relapsing forms of multiple sclerosis. The active ingredient, Glatiramer Acetate, is a random polymer of 4 amino acids found in myelin basic protein (glutamic acid, lysine, alanine and tyrosine). The applicable subheading for the Glatiramer Acetate injection in 20mg/mL and 40mg/mL single dose pre-filled syringes will be 3004.90.9215, Harmonized Tariff Schedule of the United States…
H252416 · 2016-05-02 — Tariff classification of Sirolimus tablets, imported in dosage form
S. Customs and Border Protection (CBP) National Commodity Specialist Division (NCSD) in New York, on behalf of Zydus Pharmaceuticals (USA), Inc. (Zydus), seeking a prospective ruling under the Harmonized Tariff Schedule of the United States (HTSUS), regarding the tariff classification of Sirolimus tablets. Your request was forwarded to this office for a response. No samples were provided to this office, but a sample was provided by Zydus to CBP’s Laboratories and Scientific Services for analysis. FACTS: The subject merchandise is described in your ruling request as sirolimus tablets, in 0.5…
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