NDC 71335-1517 – Ibuprofen

Ibuprofen 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1517

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090796
Marketed since
December 30, 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 (9)

Package NDCDescriptionSince
71335-1517-120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1)Feb 20, 2020
71335-1517-230 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2)Feb 20, 2020
71335-1517-340 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3)Feb 20, 2020
71335-1517-460 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4)Feb 20, 2020
71335-1517-590 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5)Feb 20, 2020
71335-1517-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6)Feb 20, 2020
71335-1517-7100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7)Feb 20, 2020
71335-1517-821 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8)Feb 20, 2020
71335-1517-915 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9)Feb 20, 2020

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