NDC 71335-1207 – Ibuprofen

Ibuprofen 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1207

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
71335-1207-021 TABLET, FILM COATED in 1 BOTTLE (71335-1207-0)Oct 30, 2019
71335-1207-120 TABLET, FILM COATED in 1 BOTTLE (71335-1207-1)Dec 26, 2019
71335-1207-215 TABLET, FILM COATED in 1 BOTTLE (71335-1207-2)Sep 4, 2020
71335-1207-330 TABLET, FILM COATED in 1 BOTTLE (71335-1207-3)May 6, 2019
71335-1207-440 TABLET, FILM COATED in 1 BOTTLE (71335-1207-4)Jul 29, 2020
71335-1207-560 TABLET, FILM COATED in 1 BOTTLE (71335-1207-5)Apr 15, 2019
71335-1207-690 TABLET, FILM COATED in 1 BOTTLE (71335-1207-6)Nov 20, 2019
71335-1207-7120 TABLET, FILM COATED in 1 BOTTLE (71335-1207-7)Sep 4, 2020
71335-1207-850 TABLET, FILM COATED in 1 BOTTLE (71335-1207-8)Sep 4, 2020
71335-1207-9100 TABLET, FILM COATED in 1 BOTTLE (71335-1207-9)Jan 22, 2020

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