FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 10135-838 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMarlex Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215435
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20260701
Package count2

External sources

Source: openFDA. Public-domain (CC0).