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Eszopiclone

NDC 68788-7029 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202929
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESZOPICLONE (2 mg/1)
Marketing started20171012
Package count5

External sources

Source: openFDA. Public-domain (CC0).