FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 70010-028 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213186
Dosage form / routeTABLET · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20201001
Package count3

External sources

Source: openFDA. Public-domain (CC0).