NDC 71205-239 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-239

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA085161
Marketed since
January 1, 1990
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (13)

Package NDCDescriptionSince
71205-239-055 TABLET in 1 BOTTLE (71205-239-05)Mar 1, 2019
71205-239-066 TABLET in 1 BOTTLE (71205-239-06)Mar 1, 2019
71205-239-077 TABLET in 1 BOTTLE (71205-239-07)Mar 1, 2019
71205-239-1010 TABLET in 1 BOTTLE (71205-239-10)Mar 1, 2019
71205-239-1212 TABLET in 1 BOTTLE (71205-239-12)Mar 1, 2019
71205-239-1414 TABLET in 1 BOTTLE (71205-239-14)Mar 1, 2019
71205-239-1515 TABLET in 1 BOTTLE (71205-239-15)Mar 1, 2019
71205-239-1818 TABLET in 1 BOTTLE (71205-239-18)Mar 1, 2019
71205-239-2020 TABLET in 1 BOTTLE (71205-239-20)Mar 1, 2019
71205-239-2121 TABLET in 1 BOTTLE (71205-239-21)Mar 1, 2019
71205-239-3030 TABLET in 1 BOTTLE (71205-239-30)Mar 1, 2019
71205-239-6060 TABLET in 1 BOTTLE (71205-239-60)Mar 1, 2019
71205-239-9090 TABLET in 1 BOTTLE (71205-239-90)Mar 1, 2019

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