NDC 71335-1911 – Ibuprofen

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

Human Otc Drug

Product NDC71335-1911

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
September 20, 2018
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
71335-1911-090 TABLET, FILM COATED in 1 BOTTLE (71335-1911-0)Jul 15, 2021
71335-1911-120 TABLET, FILM COATED in 1 BOTTLE (71335-1911-1)Jul 15, 2021
71335-1911-215 TABLET, FILM COATED in 1 BOTTLE (71335-1911-2)Jul 15, 2021
71335-1911-330 TABLET, FILM COATED in 1 BOTTLE (71335-1911-3)Jul 15, 2021
71335-1911-4100 TABLET, FILM COATED in 1 BOTTLE (71335-1911-4)Jul 15, 2021
71335-1911-560 TABLET, FILM COATED in 1 BOTTLE (71335-1911-5)Jul 15, 2021
71335-1911-650 TABLET, FILM COATED in 1 BOTTLE (71335-1911-6)Jul 15, 2021
71335-1911-740 TABLET, FILM COATED in 1 BOTTLE (71335-1911-7)Jul 15, 2021
71335-1911-810 TABLET, FILM COATED in 1 BOTTLE (71335-1911-8)Jul 15, 2021
71335-1911-956 TABLET, FILM COATED in 1 BOTTLE (71335-1911-9)Jul 15, 2021

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