Label: FAMOTIDINE powder
- NDC Code(s): 73377-057-01, 73377-057-02
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated January 11, 2021
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- Official Label (Printer Friendly)
- Famotidine
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INGREDIENTS AND APPEARANCE
FAMOTIDINE
famotidine powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:73377-057 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) FAMOTIDINE 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:73377-057-01 500 g in 1 JAR 06/10/2020 2 NDC:73377-057-02 10000 g in 1 DRUM 01/11/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 06/10/2020 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack(73377-057) , relabel(73377-057)
