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Prednisone

NDC 80425-0486 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211575
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (20 mg/1)
Marketing started20250317
Package count5

External sources

Source: openFDA. Public-domain (CC0).