NDC 71335-2752 – PredniSONE Tablets, USP, 10 mg

Prednisone 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2752

Product details

Brand name
PredniSONE Tablets, USP, 10 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, 10 mg →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2752-010 TABLET in 1 BOTTLE (71335-2752-0)Oct 3, 2025
71335-2752-121 TABLET in 1 BOTTLE (71335-2752-1)Oct 3, 2025
71335-2752-240 TABLET in 1 BOTTLE (71335-2752-2)Oct 3, 2025
71335-2752-330 TABLET in 1 BOTTLE (71335-2752-3)Oct 3, 2025
71335-2752-420 TABLET in 1 BOTTLE (71335-2752-4)Oct 3, 2025
71335-2752-515 TABLET in 1 BOTTLE (71335-2752-5)Oct 3, 2025
71335-2752-650 TABLET in 1 BOTTLE (71335-2752-6)Oct 3, 2025
71335-2752-760 TABLET in 1 BOTTLE (71335-2752-7)Oct 3, 2025
71335-2752-842 TABLET in 1 BOTTLE (71335-2752-8)Oct 3, 2025
71335-2752-948 TABLET in 1 BOTTLE (71335-2752-9)Oct 3, 2025

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