Label: BUDESONIDE powder
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- NDC Code(s): 73377-005-01, 73377-005-02, 73377-005-03
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated May 3, 2021
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- Budesonide
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INGREDIENTS AND APPEARANCE
BUDESONIDE
budesonide powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:73377-005 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BUDESONIDE (UNII: Q3OKS62Q6X) (BUDESONIDE - UNII:Q3OKS62Q6X) BUDESONIDE 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:73377-005-01 500 g in 1 JAR 01/23/2020 2 NDC:73377-005-02 100 g in 1 JAR 09/01/2020 3 NDC:73377-005-03 25 g in 1 JAR 05/03/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 01/23/2020 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack(73377-005) , relabel(73377-005)
