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Ketoconazole

NDC 51672-4026 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075319
Dosage form / routeTABLET · ORAL
Active ingredientsKETOCONAZOLE (200 mg/1)
Marketing started19990615
Package count6

External sources

Source: openFDA. Public-domain (CC0).