Label: BENAZEPRIL HYDROCHLORIDE powder
- NDC Code(s): 73377-060-01, 73377-060-02
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated July 9, 2020
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- Official Label (Printer Friendly)
- Benazepril Hydrochloride
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INGREDIENTS AND APPEARANCE
BENAZEPRIL HYDROCHLORIDE
benazepril hydrochloride powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:73377-060 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T) (BENAZEPRIL HYDROCHLORIDE - UNII:N1SN99T69T) BENAZEPRIL HYDROCHLORIDE 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:73377-060-01 500 g in 1 JAR 07/09/2020 2 NDC:73377-060-02 100 g in 1 JAR 07/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 07/09/2020 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack(73377-060) , relabel(73377-060)
