NDC 68071-3617 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3617

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211575
Marketed since
November 15, 2019
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (5)

Package NDCDescriptionSince
68071-3617-110 TABLET in 1 BOTTLE (68071-3617-1)Jun 19, 2024
68071-3617-414 TABLET in 1 BOTTLE (68071-3617-4)Jun 19, 2024
68071-3617-660 TABLET in 1 BOTTLE (68071-3617-6)Nov 8, 2024
68071-3617-721 TABLET in 1 BOTTLE (68071-3617-7)Oct 16, 2024
68071-3617-88 TABLET in 1 BOTTLE (68071-3617-8)Jun 19, 2024

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