Label: ONDANSETRON HCL DIHYDRATE powder
- NDC Code(s): 73377-325-01, 73377-325-02
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT - ANIMAL DRUG
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated September 17, 2025
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- Official Label (Printer Friendly)
- Ondansetron HCl Dihydrate
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INGREDIENTS AND APPEARANCE
ONDANSETRON HCL DIHYDRATE
ondansetron hcl dihydrate powderProduct Information Product Type Item Code (Source) NDC:73377-325 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONDANSETRON HYDROCHLORIDE (UNII: NMH84OZK2B) (ONDANSETRON - UNII:4AF302ESOS) ONDANSETRON 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:73377-325-01 100 g in 1 JAR 2 NDC:73377-325-02 500 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 06/20/2025 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 label, pack, relabel, repack Establishment Name Address ID/FEI Business Operations NATCO PHARMA LIMITED 862497174 api manufacture
