Label: CIPROFLOXACIN HYDROCHLORIDE powder
- NDC Code(s): 73377-158-01, 73377-158-02
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT - ANIMAL DRUG
Drug Label Information
Updated March 9, 2022
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- Official Label (Printer Friendly)
- Ciprofloxacin Hydrochloride
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INGREDIENTS AND APPEARANCE
CIPROFLOXACIN HYDROCHLORIDE
ciprofloxacin hydrochloride powderProduct Information Product Type Item Code (Source) NDC:73377-158 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CIPROFLOXACIN HYDROCHLORIDE (UNII: 4BA73M5E37) (CIPROFLOXACIN - UNII:5E8K9I0O4U) CIPROFLOXACIN 1 g in 1 g Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73377-158-01 1000 g in 1 JAR 2 NDC:73377-158-02 50 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 03/09/2022 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack, relabel
