FDA NDC Directory · JSON-LD · Markdown

Carbidopa and Levodopa

NDC 77771-461 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerRadha Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA214091
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsCARBIDOPA (50 mg/1)
LEVODOPA (200 mg/1)
Marketing started20250425
Package count1

External sources

Source: openFDA. Public-domain (CC0).