NDC 71335-2068 – Ibuprofen

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

Human Otc Drug

Product NDC71335-2068

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA072096
Marketed since
August 16, 1994
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
71335-2068-090 TABLET, FILM COATED in 1 BOTTLE (71335-2068-0)Mar 29, 2022
71335-2068-120 TABLET, FILM COATED in 1 BOTTLE (71335-2068-1)Mar 29, 2022
71335-2068-215 TABLET, FILM COATED in 1 BOTTLE (71335-2068-2)Mar 29, 2022
71335-2068-330 TABLET, FILM COATED in 1 BOTTLE (71335-2068-3)Mar 29, 2022
71335-2068-4100 TABLET, FILM COATED in 1 BOTTLE (71335-2068-4)Mar 29, 2022
71335-2068-560 TABLET, FILM COATED in 1 BOTTLE (71335-2068-5)Mar 29, 2022
71335-2068-650 TABLET, FILM COATED in 1 BOTTLE (71335-2068-6)Mar 29, 2022
71335-2068-740 TABLET, FILM COATED in 1 BOTTLE (71335-2068-7)Mar 29, 2022
71335-2068-810 TABLET, FILM COATED in 1 BOTTLE (71335-2068-8)Mar 29, 2022
71335-2068-956 TABLET, FILM COATED in 1 BOTTLE (71335-2068-9)Mar 29, 2022

Other Ibuprofen products