NDC 71335-1206 – Ibuprofen

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

Human Prescription Drug

Product NDC71335-1206

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078329
Marketed since
August 24, 2018
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1206-084 TABLET, FILM COATED in 1 BOTTLE (71335-1206-0)May 6, 2019
71335-1206-120 TABLET, FILM COATED in 1 BOTTLE (71335-1206-1)Sep 5, 2019
71335-1206-215 TABLET, FILM COATED in 1 BOTTLE (71335-1206-2)May 6, 2019
71335-1206-340 TABLET, FILM COATED in 1 BOTTLE (71335-1206-3)Sep 10, 2019
71335-1206-421 TABLET, FILM COATED in 1 BOTTLE (71335-1206-4)Sep 25, 2019
71335-1206-530 TABLET, FILM COATED in 1 BOTTLE (71335-1206-5)May 8, 2019
71335-1206-690 TABLET, FILM COATED in 1 BOTTLE (71335-1206-6)Oct 14, 2019
71335-1206-7100 TABLET, FILM COATED in 1 BOTTLE (71335-1206-7)Oct 10, 2019
71335-1206-8120 TABLET, FILM COATED in 1 BOTTLE (71335-1206-8)May 6, 2019
71335-1206-960 TABLET, FILM COATED in 1 BOTTLE (71335-1206-9)May 6, 2019

Other Ibuprofen products