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Mirtazapine

NDC 63739-099 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMcKesson Corporation dba SKY Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA077666
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMIRTAZAPINE (30 mg/1)
Marketing started20070822
Marketing ended20270331
Package count1

External sources

Source: openFDA. Public-domain (CC0).