FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 87063-189 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerASCLEMED USA INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215243
Dosage form / routeTABLET · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20230501
Package count7

External sources

Source: openFDA. Public-domain (CC0).