FDA NDC Directory · JSON-LD · Markdown

Carisoprodol

NDC 69367-419 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207237
Dosage form / routeTABLET · ORAL
Active ingredientsCARISOPRODOL (250 mg/1)
Marketing started20251125
Package count1

External sources

Source: openFDA. Public-domain (CC0).