FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 76420-628 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211567
Dosage form / routeTABLET · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20190723
Package count4

External sources

Source: openFDA. Public-domain (CC0).