FDA NDC Directory · JSON-LD · Markdown

Miglitol

NDC 71205-937 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203965
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMIGLITOL (100 mg/1)
Marketing started20210115
Package count4

External sources

Source: openFDA. Public-domain (CC0).