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Pentoxifylline

NDC 70954-668 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074878
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPENTOXIFYLLINE (400 mg/1)
Marketing started20240115
Package count2

External sources

Source: openFDA. Public-domain (CC0).