FDA NDC Directory · JSON-LD · Markdown

Mirtazapine

NDC 70954-830 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219919
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMIRTAZAPINE (7.5 mg/1)
Marketing started20260514
Package count1

External sources

Source: openFDA. Public-domain (CC0).