FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 43598-741 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr.Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA091693
Dosage form / routeTABLET · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20190722
Marketing ended20260731
Package count2

External sources

Source: openFDA. Public-domain (CC0).