NDC 71335-1503 – Ibuprofen

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

Human Prescription Drug

Product NDC71335-1503

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 (10)

Package NDCDescriptionSince
71335-1503-021 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0)Feb 12, 2020
71335-1503-120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-1)Feb 12, 2020
71335-1503-215 TABLET, FILM COATED in 1 BOTTLE (71335-1503-2)Feb 12, 2020
71335-1503-330 TABLET, FILM COATED in 1 BOTTLE (71335-1503-3)Feb 12, 2020
71335-1503-440 TABLET, FILM COATED in 1 BOTTLE (71335-1503-4)Feb 12, 2020
71335-1503-560 TABLET, FILM COATED in 1 BOTTLE (71335-1503-5)Feb 12, 2020
71335-1503-690 TABLET, FILM COATED in 1 BOTTLE (71335-1503-6)Feb 12, 2020
71335-1503-7120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-7)Feb 12, 2020
71335-1503-850 TABLET, FILM COATED in 1 BOTTLE (71335-1503-8)Feb 12, 2020
71335-1503-9100 TABLET, FILM COATED in 1 BOTTLE (71335-1503-9)Feb 12, 2020

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