Label: DIAZOXIDE powder
- NDC Code(s): 73377-056-01, 73377-056-02, 73377-056-03
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
Drug Label Information
Updated August 18, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Diazoxide
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INGREDIENTS AND APPEARANCE
DIAZOXIDE
diazoxide powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:73377-056 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIAZOXIDE (UNII: O5CB12L4FN) (DIAZOXIDE - UNII:O5CB12L4FN) DIAZOXIDE 1 g in 1 g Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73377-056-01 500 g in 1 JAR 06/08/2020 2 NDC:73377-056-02 1000 g in 1 JAR 06/17/2020 3 NDC:73377-056-03 100 g in 1 JAR 08/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 06/08/2020 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack(73377-056) , relabel(73377-056)
