Budesonide: Package Insert and Label Information

BUDESONIDE- budesonide powder
AX Pharmaceutical Corp

Budesonide

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BUDESONIDE
budesonide powder
Product Information
Product Type BULK INGREDIENT Item Code (Source) NDC:73377-005
Route of Administration NOT APPLICABLE DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BUDESONIDE (BUDESONIDE) BUDESONIDE 1 g in 1 g
Product Characteristics
Color white Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:73377-005-01 500 g in 1 JAR None
2 NDC:73377-005-02 100 g in 1 JAR None
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 Operations
AX Pharmaceutical Corp 204011316 repack (73377-005), relabel (73377-005)

Revised: 09/2020 AX Pharmaceutical Corp

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