Label: CROMOLYN SODIUM powder
- NDC Code(s): 73377-122-01
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated April 5, 2021
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- Official Label (Printer Friendly)
- Cromolyn sodium
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INGREDIENTS AND APPEARANCE
CROMOLYN SODIUM
cromolyn sodium powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:73377-122 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CROMOLYN SODIUM (UNII: Q2WXR1I0PK) (CROMOLYN SODIUM - UNII:Q2WXR1I0PK) CROMOLYN SODIUM 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:73377-122-01 100 g in 1 JAR 04/05/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 04/05/2021 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack(73377-122) , relabel(73377-122)
