NDC 63629-1467 – Ibuprofen

Ibuprofen 200 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC63629-1467

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075010
Marketed since
January 1, 2004
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (10)

Package NDCDescriptionSince
63629-1467-090 TABLET, FILM COATED in 1 BOTTLE (63629-1467-0)Nov 20, 2013
63629-1467-120 TABLET, FILM COATED in 1 BOTTLE (63629-1467-1)Jul 15, 2005
63629-1467-215 TABLET, FILM COATED in 1 BOTTLE (63629-1467-2)Jun 19, 2017
63629-1467-330 TABLET, FILM COATED in 1 BOTTLE (63629-1467-3)Jan 17, 2005
63629-1467-4100 TABLET, FILM COATED in 1 BOTTLE (63629-1467-4)Feb 21, 2006
63629-1467-560 TABLET, FILM COATED in 1 BOTTLE (63629-1467-5)Feb 10, 2006
63629-1467-650 TABLET, FILM COATED in 1 BOTTLE (63629-1467-6)Jan 15, 2009
63629-1467-740 TABLET, FILM COATED in 1 BOTTLE (63629-1467-7)Jun 6, 2008
63629-1467-810 TABLET, FILM COATED in 1 BOTTLE (63629-1467-8)Jun 14, 2010
63629-1467-956 TABLET, FILM COATED in 1 BOTTLE (63629-1467-9)Oct 29, 2010

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