NDC 71205-741 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-741

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208412
Marketed since
September 1, 2021
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (8)

Package NDCDescriptionSince
71205-741-077 TABLET in 1 BOTTLE, PLASTIC (71205-741-07)Apr 30, 2026
71205-741-1010 TABLET in 1 BOTTLE, PLASTIC (71205-741-10)Jan 6, 2023
71205-741-1414 TABLET in 1 BOTTLE, PLASTIC (71205-741-14)Jan 6, 2023
71205-741-1515 TABLET in 1 BOTTLE, PLASTIC (71205-741-15)Jan 6, 2023
71205-741-1818 TABLET in 1 BOTTLE, PLASTIC (71205-741-18)Nov 20, 2024
71205-741-2020 TABLET in 1 BOTTLE, PLASTIC (71205-741-20)Jan 6, 2023
71205-741-2121 TABLET in 1 BOTTLE, PLASTIC (71205-741-21)Jan 6, 2023
71205-741-3030 TABLET in 1 BOTTLE, PLASTIC (71205-741-30)Jan 6, 2023

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