NDC 71335-3121 – Ibuprofen

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

Human Prescription Drug

Product NDC71335-3121

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202413
Marketed since
May 23, 2024
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
71335-3121-021 TABLET, FILM COATED in 1 BOTTLE (71335-3121-0)Apr 13, 2026
71335-3121-120 TABLET, FILM COATED in 1 BOTTLE (71335-3121-1)Apr 13, 2026
71335-3121-215 TABLET, FILM COATED in 1 BOTTLE (71335-3121-2)Apr 13, 2026
71335-3121-330 TABLET, FILM COATED in 1 BOTTLE (71335-3121-3)Apr 13, 2026
71335-3121-440 TABLET, FILM COATED in 1 BOTTLE (71335-3121-4)Apr 13, 2026
71335-3121-560 TABLET, FILM COATED in 1 BOTTLE (71335-3121-5)Apr 13, 2026
71335-3121-690 TABLET, FILM COATED in 1 BOTTLE (71335-3121-6)Apr 13, 2026
71335-3121-7120 TABLET, FILM COATED in 1 BOTTLE (71335-3121-7)Apr 13, 2026
71335-3121-850 TABLET, FILM COATED in 1 BOTTLE (71335-3121-8)Apr 13, 2026
71335-3121-9100 TABLET, FILM COATED in 1 BOTTLE (71335-3121-9)Apr 13, 2026

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