NDC 71335-1073 – Ibuprofen

Ibuprofen 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1073

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091625
Marketed since
December 21, 2015
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
71335-1073-084 TABLET, FILM COATED in 1 BOTTLE (71335-1073-0)Dec 28, 2021
71335-1073-120 TABLET, FILM COATED in 1 BOTTLE (71335-1073-1)Feb 14, 2019
71335-1073-215 TABLET, FILM COATED in 1 BOTTLE (71335-1073-2)Feb 13, 2019
71335-1073-340 TABLET, FILM COATED in 1 BOTTLE (71335-1073-3)Feb 26, 2019
71335-1073-421 TABLET, FILM COATED in 1 BOTTLE (71335-1073-4)Feb 14, 2019
71335-1073-530 TABLET, FILM COATED in 1 BOTTLE (71335-1073-5)Jun 6, 2019
71335-1073-690 TABLET, FILM COATED in 1 BOTTLE (71335-1073-6)Feb 21, 2019
71335-1073-7100 TABLET, FILM COATED in 1 BOTTLE (71335-1073-7)Feb 19, 2019
71335-1073-8120 TABLET, FILM COATED in 1 BOTTLE (71335-1073-8)Jul 18, 2019
71335-1073-960 TABLET, FILM COATED in 1 BOTTLE (71335-1073-9)Feb 27, 2019

Other Ibuprofen products