FDA NDC Directory · JSON-LD · Markdown

RAMELTEON

NDC 72189-153 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA211567
Dosage form / routeTABLET · ORAL
Active ingredientsRAMELTEON (8 mg/1)
Marketing started20201103
Package count1

External sources

Source: openFDA. Public-domain (CC0).