NDC 71335-3047 – PredniSONE Tablets, USP, 20 mg

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3047

Product details

Brand name
PredniSONE Tablets, USP, 20 mg
Generic name
PredniSONE
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212629
Marketed since
May 22, 2025
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for PredniSONE Tablets, USP, 20 mg →

Package NDC codes (1)

Package NDCDescriptionSince
71335-3047-11000 TABLET in 1 BOTTLE (71335-3047-1)Dec 3, 2025

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