NDC 70518-4293 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4293

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208412
Marketed since
February 26, 2025
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (8)

Package NDCDescriptionSince
70518-4293-010 TABLET in 1 BOTTLE, PLASTIC (70518-4293-0)Feb 26, 2025
70518-4293-17 TABLET in 1 BOTTLE, PLASTIC (70518-4293-1)Aug 27, 2025
70518-4293-25 TABLET in 1 BOTTLE, PLASTIC (70518-4293-2)Oct 11, 2025
70518-4293-314 TABLET in 1 BOTTLE, PLASTIC (70518-4293-3)Oct 15, 2025
70518-4293-430 TABLET in 1 BOTTLE, PLASTIC (70518-4293-4)Nov 22, 2025
70518-4293-56 TABLET in 1 BOTTLE, PLASTIC (70518-4293-5)Feb 17, 2026
70518-4293-65 TABLET in 1 BOTTLE, PLASTIC (70518-4293-6)Feb 17, 2026
70518-4293-78 TABLET in 1 BOTTLE, PLASTIC (70518-4293-7)Aug 25, 2026

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