Label: BENAZEPRIL HYDROCHLORIDE powder
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NDC Code(s):
73377-060-01,
73377-060-02,
73377-060-03,
73377-060-04, view more73377-060-05
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT - ANIMAL DRUG
- DEA Schedule: None
- Marketing Status: bulk ingredient
Drug Label Information
Updated January 22, 2025
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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 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 2 NDC:73377-060-02 100 g in 1 JAR 3 NDC:73377-060-03 1000 g in 1 JAR 4 NDC:73377-060-04 50 g in 1 JAR 5 NDC:73377-060-05 92 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient 07/09/2020 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack, relabel