NDC 71335-2753 – PredniSONE Tablets, USP, 5 mg

Prednisone 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2753

Product details

Brand name
PredniSONE Tablets, USP, 5 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, 5 mg →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2753-042 TABLET in 1 BOTTLE (71335-2753-0)Oct 3, 2025
71335-2753-130 TABLET in 1 BOTTLE (71335-2753-1)Oct 3, 2025
71335-2753-278 TABLET in 1 BOTTLE (71335-2753-2)Oct 3, 2025
71335-2753-336 TABLET in 1 BOTTLE (71335-2753-3)Oct 3, 2025
71335-2753-421 TABLET in 1 BOTTLE (71335-2753-4)Oct 3, 2025
71335-2753-515 TABLET in 1 BOTTLE (71335-2753-5)Oct 3, 2025
71335-2753-6100 TABLET in 1 BOTTLE (71335-2753-6)Oct 3, 2025
71335-2753-720 TABLET in 1 BOTTLE (71335-2753-7)Oct 3, 2025
71335-2753-810 TABLET in 1 BOTTLE (71335-2753-8)Oct 3, 2025
71335-2753-990 TABLET in 1 BOTTLE (71335-2753-9)Oct 3, 2025

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