FDA NDC Directory · JSON-LD · Markdown

CARBINOXAMINE MALEATE

NDC 69315-239 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215476
Dosage form / routeTABLET · ORAL
Active ingredientsCARBINOXAMINE MALEATE (6 mg/1)
Marketing started20250801
Package count1

External sources

Source: openFDA. Public-domain (CC0).