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Clozapine

NDC 59651-263 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA212923
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsCLOZAPINE (150 mg/1)
Marketing started20241212
Package count2

External sources

Source: openFDA. Public-domain (CC0).