Label: OXIBENDAZOLE powder
- NDC Code(s): 72969-117-10
- Packager: PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated December 21, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
OXIBENDAZOLE
oxibendazole powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:72969-117 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXIBENDAZOLE (UNII: 022N12KJ0X) (OXIBENDAZOLE - UNII:022N12KJ0X) OXIBENDAZOLE 1 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72969-117-10 1 g in 1 PACKAGE 12/19/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 12/19/2021 Labeler - PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC (080173485)