Label: GEFITINIB powder
- NDC Code(s): 73377-121-01
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated April 12, 2021
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- Official Label (Printer Friendly)
- Gefitinib
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INGREDIENTS AND APPEARANCE
GEFITINIB
gefitinib powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:73377-121 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GEFITINIB (UNII: S65743JHBS) (GEFITINIB - UNII:S65743JHBS) GEFITINIB 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:73377-121-01 100 g in 1 JAR 04/12/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 04/12/2021 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 relabel(73377-121) , repack(73377-121)
