FDA NDC Directory · JSON-LD · Markdown

ESZOPICLONE

NDC 47335-588 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091103
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESZOPICLONE (3 mg/1)
Marketing started20140415
Package count4

External sources

Source: openFDA. Public-domain (CC0).