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PredniSONE Tablets, USP, 20 mg

NDC 63561-0122 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePredniSONE
Labeler / ManufacturerGranulation Technology, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212629
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (20 mg/1)
Marketing started20250522
Package count3

External sources

Source: openFDA. Public-domain (CC0).