NDC 68071-3738 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3738

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215672
Marketed since
March 28, 2022
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (4)

Package NDCDescriptionSince
68071-3738-110 TABLET in 1 BOTTLE (68071-3738-1)Jan 21, 2025
68071-3738-33 TABLET in 1 BOTTLE (68071-3738-3)Jul 21, 2026
68071-3738-44 TABLET in 1 BOTTLE (68071-3738-4)Jul 30, 2025
68071-3738-66 TABLET in 1 BOTTLE (68071-3738-6)Dec 5, 2024

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