FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 52817-235 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTruPharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212650
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20200630
Package count2

External sources

Source: openFDA. Public-domain (CC0).