NDC 71335-1396 – Ibuprofen

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

Human Prescription Drug

Product NDC71335-1396

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
71335-1396-084 TABLET, FILM COATED in 1 BOTTLE (71335-1396-0)Nov 18, 2019
71335-1396-120 TABLET, FILM COATED in 1 BOTTLE (71335-1396-1)Nov 18, 2019
71335-1396-215 TABLET, FILM COATED in 1 BOTTLE (71335-1396-2)Nov 18, 2019
71335-1396-340 TABLET, FILM COATED in 1 BOTTLE (71335-1396-3)Nov 18, 2019
71335-1396-421 TABLET, FILM COATED in 1 BOTTLE (71335-1396-4)Nov 18, 2019
71335-1396-530 TABLET, FILM COATED in 1 BOTTLE (71335-1396-5)Nov 18, 2019
71335-1396-690 TABLET, FILM COATED in 1 BOTTLE (71335-1396-6)Nov 18, 2019
71335-1396-7100 TABLET, FILM COATED in 1 BOTTLE (71335-1396-7)Nov 18, 2019
71335-1396-8120 TABLET, FILM COATED in 1 BOTTLE (71335-1396-8)Nov 18, 2019
71335-1396-960 TABLET, FILM COATED in 1 BOTTLE (71335-1396-9)Nov 18, 2019

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