NDC 72162-2486 – PredniSONE Tablets, USP, 20 mg

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2486

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
March 6, 2024
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 (2)

Package NDCDescriptionSince
72162-2486-01000 TABLET in 1 BOTTLE (72162-2486-0)May 5, 2025
72162-2486-1100 TABLET in 1 BOTTLE (72162-2486-1)May 5, 2025

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