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Mirtazapine

NDC 66993-607 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPrasco Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA216751
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMIRTAZAPINE (15 mg/1)
Marketing started20230901
Package count2

External sources

Source: openFDA. Public-domain (CC0).