FDA NDC Directory · JSON-LD · Markdown

Misoprostol

NDC 50268-555 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA210201
Dosage form / routeTABLET · ORAL
Active ingredientsMISOPROSTOL (200 ug/1)
Marketing started20241003
Package count1

External sources

Source: openFDA. Public-domain (CC0).