NDC 63629-1605 – Prednisone

Prednisone 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-1605

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040256
Marketed since
July 12, 2002
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (10)

Package NDCDescriptionSince
63629-1605-042 TABLET in 1 BOTTLE (63629-1605-0)Jun 8, 2010
63629-1605-130 TABLET in 1 BOTTLE (63629-1605-1)Dec 7, 2004
63629-1605-278 TABLET in 1 BOTTLE (63629-1605-2)Mar 18, 2005
63629-1605-336 TABLET in 1 BOTTLE (63629-1605-3)Mar 12, 2010
63629-1605-421 TABLET in 1 BOTTLE (63629-1605-4)Jan 10, 2005
63629-1605-515 TABLET in 1 BOTTLE (63629-1605-5)Feb 11, 2005
63629-1605-6100 TABLET in 1 BOTTLE (63629-1605-6)Sep 15, 2008
63629-1605-720 TABLET in 1 BOTTLE (63629-1605-7)Jun 15, 2009
63629-1605-810 TABLET in 1 BOTTLE (63629-1605-8)Jan 18, 2010
63629-1605-990 TABLET in 1 BOTTLE (63629-1605-9)Apr 20, 2010

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