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Prednisone

NDC 80425-0193 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx Pharmacy of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040362
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (10 mg/1)
Marketing started20220620
Package count1

External sources

Source: openFDA. Public-domain (CC0).