FDA NDC Directory · JSON-LD · Markdown

Carbidopa and Levodopa

NDC 69367-340 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214092
Dosage form / routeTABLET · ORAL
Active ingredientsCARBIDOPA (25 mg/1)
LEVODOPA (250 mg/1)
Marketing started20210930
Package count2

External sources

Source: openFDA. Public-domain (CC0).