FDA NDC Directory · JSON-LD · Markdown

Ramelteon

NDC 80425-0593 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215243
Dosage form / routeTABLET · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20260727
Package count1

External sources

Source: openFDA. Public-domain (CC0).