NDC 63187-807 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-807

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040362
Marketed since
August 29, 2001
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (16)

Package NDCDescriptionSince
63187-807-055 TABLET in 1 BOTTLE (63187-807-05)Feb 1, 2017
63187-807-066 TABLET in 1 BOTTLE (63187-807-06)Feb 1, 2017
63187-807-077 TABLET in 1 BOTTLE (63187-807-07)Apr 3, 2017
63187-807-088 TABLET in 1 BOTTLE (63187-807-08)Feb 1, 2017
63187-807-099 TABLET in 1 BOTTLE (63187-807-09)Feb 1, 2017
63187-807-1010 TABLET in 1 BOTTLE (63187-807-10)Feb 1, 2017
63187-807-1212 TABLET in 1 BOTTLE (63187-807-12)Feb 1, 2017
63187-807-1414 TABLET in 1 BOTTLE (63187-807-14)Nov 1, 2018
63187-807-1515 TABLET in 1 BOTTLE (63187-807-15)Feb 1, 2017
63187-807-1818 TABLET in 1 BOTTLE (63187-807-18)Mar 1, 2018
63187-807-2020 TABLET in 1 BOTTLE (63187-807-20)Feb 1, 2017
63187-807-2121 TABLET in 1 BOTTLE (63187-807-21)Feb 1, 2017
63187-807-2424 TABLET in 1 BOTTLE (63187-807-24)Feb 1, 2017
63187-807-3030 TABLET in 1 BOTTLE (63187-807-30)Feb 1, 2017
63187-807-4040 TABLET in 1 BOTTLE (63187-807-40)Feb 1, 2017
63187-807-4242 TABLET in 1 BOTTLE (63187-807-42)Feb 1, 2017

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