FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 72319-005 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / Manufactureri3 Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212650
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20200430
Package count3

External sources

Source: openFDA. Public-domain (CC0).