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prednisone

NDC 0615-8438 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePREDNISONE
Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA210785
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (1 mg/1)
Marketing started20210901
Package count1

External sources

Source: openFDA. Public-domain (CC0).