NDC 71335-2079 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2079

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208412
Marketed since
September 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2079-011 TABLET in 1 BOTTLE, PLASTIC (71335-2079-0)May 3, 2022
71335-2079-120 TABLET in 1 BOTTLE, PLASTIC (71335-2079-1)May 6, 2022
71335-2079-230 TABLET in 1 BOTTLE, PLASTIC (71335-2079-2)May 31, 2022
71335-2079-340 TABLET in 1 BOTTLE, PLASTIC (71335-2079-3)Sep 6, 2022
71335-2079-415 TABLET in 1 BOTTLE, PLASTIC (71335-2079-4)Jun 9, 2022
71335-2079-510 TABLET in 1 BOTTLE, PLASTIC (71335-2079-5)Apr 27, 2022
71335-2079-621 TABLET in 1 BOTTLE, PLASTIC (71335-2079-6)Jun 2, 2022
71335-2079-718 TABLET in 1 BOTTLE, PLASTIC (71335-2079-7)Jun 23, 2022
71335-2079-812 TABLET in 1 BOTTLE, PLASTIC (71335-2079-8)Apr 18, 2022
71335-2079-923 TABLET in 1 BOTTLE, PLASTIC (71335-2079-9)Apr 3, 2024

Other Prednisone products