NDC 68071-3721 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3721

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 (8)

Package NDCDescriptionSince
68071-3721-010 TABLET in 1 BOTTLE (68071-3721-0)Dec 4, 2024
68071-3721-118 TABLET in 1 BOTTLE (68071-3721-1)Dec 19, 2024
68071-3721-220 TABLET in 1 BOTTLE (68071-3721-2)Nov 20, 2024
68071-3721-330 TABLET in 1 BOTTLE (68071-3721-3)Mar 3, 2025
68071-3721-414 TABLET in 1 BOTTLE (68071-3721-4)Feb 27, 2026
68071-3721-515 TABLET in 1 BOTTLE (68071-3721-5)Dec 2, 2024
68071-3721-721 TABLET in 1 BOTTLE (68071-3721-7)Mar 3, 2025
68071-3721-88 TABLET in 1 BOTTLE (68071-3721-8)Dec 10, 2024

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