Ondansetron HCl Dihydrate
Ondansetron HCl Dihydrate
Approved
Approval ID
90987762-202d-4e46-a37f-936f1f7ce381
Product Type
BULK INGREDIENT - ANIMAL DRUG
Effective Date
Sep 17, 2025
Manufacturers
FDA
AX Pharmaceutical Corp
DUNS: 204011316
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ondansetron HCl Dihydrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code73377-325
Product Classification
G
Generic Name
Ondansetron HCl Dihydrate
Product Specifications
Route of AdministrationNOT APPLICABLE
Effective DateSeptember 17, 2025
FDA Product Classification
INGREDIENTS (1)
ONDANSETRON HYDROCHLORIDEActive
Quantity: 1 g in 1 g
Code: NMH84OZK2B
Classification: ACTIM
Drug Labeling Information
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
LOINC: 51945-4Updated: 9/17/2025
Ondansetron HCl Dihydrate
