NDC 71205-089 – Prednisone

Prednisone 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-089

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040611
Marketed since
June 6, 2005
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (17)

Package NDCDescriptionSince
71205-089-00100 TABLET in 1 BOTTLE (71205-089-00)Aug 1, 2018
71205-089-055 TABLET in 1 BOTTLE (71205-089-05)Aug 1, 2018
71205-089-066 TABLET in 1 BOTTLE (71205-089-06)Aug 1, 2018
71205-089-077 TABLET in 1 BOTTLE (71205-089-07)Aug 1, 2018
71205-089-088 TABLET in 1 BOTTLE (71205-089-08)Aug 1, 2018
71205-089-1010 TABLET in 1 BOTTLE (71205-089-10)Aug 1, 2018
71205-089-1212 TABLET in 1 BOTTLE (71205-089-12)Aug 1, 2018
71205-089-1515 TABLET in 1 BOTTLE (71205-089-15)Aug 1, 2018
71205-089-1818 TABLET in 1 BOTTLE (71205-089-18)Aug 1, 2018
71205-089-2020 TABLET in 1 BOTTLE (71205-089-20)Aug 1, 2018
71205-089-2121 TABLET in 1 BOTTLE (71205-089-21)Aug 1, 2018
71205-089-2424 TABLET in 1 BOTTLE (71205-089-24)Aug 1, 2018
71205-089-2727 TABLET in 1 BOTTLE (71205-089-27)Aug 1, 2018
71205-089-3030 TABLET in 1 BOTTLE (71205-089-30)Aug 1, 2018
71205-089-3636 TABLET in 1 BOTTLE (71205-089-36)Aug 1, 2018
71205-089-4040 TABLET in 1 BOTTLE (71205-089-40)Aug 1, 2018
71205-089-4242 TABLET in 1 BOTTLE (71205-089-42)Aug 1, 2018

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