Label: DANTROLENE SODIUM powder
- NDC Code(s): 73377-075-01, 73377-075-02, 73377-075-03
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT - ANIMAL DRUG
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated January 3, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Dantrolene Sodium
-
INGREDIENTS AND APPEARANCE
DANTROLENE SODIUM
dantrolene sodium powderProduct Information Product Type Item Code (Source) NDC:73377-075 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DANTROLENE SODIUM (UNII: 287M0347EV) (DANTROLENE - UNII:F64QU97QCR) DANTROLENE SODIUM 1 g in 1 g Product Characteristics Color orange Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73377-075-01 50 g in 1 JAR 2 NDC:73377-075-02 25000 g in 1 PACKAGE 3 NDC:73377-075-03 5000 g in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 10/06/2022 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 relabel, repack Establishment Name Address ID/FEI Business Operations AZICO BIOPHORE INDIA PRIVATE LIMITED 860186984 api manufacture