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Posaconazole

NDC 16714-535 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214321
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPOSACONAZOLE (100 mg/1)
Marketing started20230402
Package count1

External sources

Source: openFDA. Public-domain (CC0).