NDC 68788-4039 – Ibuprofen

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

Human Prescription Drug

Product NDC68788-4039

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202413
Marketed since
October 13, 2025
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (7)

Package NDCDescriptionSince
68788-4039-1100 TABLET, FILM COATED in 1 BOTTLE (68788-4039-1)Oct 13, 2025
68788-4039-220 TABLET, FILM COATED in 1 BOTTLE (68788-4039-2)Oct 13, 2025
68788-4039-330 TABLET, FILM COATED in 1 BOTTLE (68788-4039-3)Oct 13, 2025
68788-4039-550 TABLET, FILM COATED in 1 BOTTLE (68788-4039-5)Oct 13, 2025
68788-4039-660 TABLET, FILM COATED in 1 BOTTLE (68788-4039-6)Oct 13, 2025
68788-4039-828 TABLET, FILM COATED in 1 BOTTLE (68788-4039-8)Oct 13, 2025
68788-4039-990 TABLET, FILM COATED in 1 BOTTLE (68788-4039-9)Oct 13, 2025

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