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Eszopiclone

NDC 55111-629 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA091024
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsESZOPICLONE (1 mg/1)
Marketing started20140415
Package count3

External sources

Source: openFDA. Public-domain (CC0).