FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 71205-918 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA213186
Dosage form / routeTABLET · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20201001
Package count6

External sources

Source: openFDA. Public-domain (CC0).