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Posaconazole

NDC 60687-523 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA212411
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPOSACONAZOLE (100 mg/1)
Marketing started20200611
Package count2

External sources

Source: openFDA. Public-domain (CC0).