Label: AMIKACIN SULFATE INJECTION, 500 MG/2ML injection
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Contains inactivated NDC Code(s)
NDC Code(s): 71309-996-05 - Packager: Safrel Pharmaceuticals, LLC.
- Category: HUMAN PRESCRIPTION DRUG LABEL
Drug Label Information
Updated January 3, 2021
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INGREDIENTS AND APPEARANCE
AMIKACIN SULFATE INJECTION, 500 MG/2ML
amikacin sulfate injection, 500 mg/2ml injectionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71309-996 Route of Administration INTRAMUSCULAR Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMIKACIN SULFATE (UNII: N6M33094FD) (AMIKACIN - UNII:84319SGC3C) AMIKACIN 500 mg Inactive Ingredients Ingredient Name Strength SULFURIC ACID (UNII: O40UQP6WCF) SODIUM METABISULFITE (UNII: 4VON5FNS3C) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71309-996-05 500 in 1 VIAL; Type 0: Not a Combination Product 08/04/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 08/01/2020 Labeler - Safrel Pharmaceuticals, LLC. (080566287)