NDC 68788-4139 – Ibuprofen

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

Human Prescription Drug

Product NDC68788-4139

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
July 6, 2026
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (5)

Package NDCDescriptionSince
68788-4139-1100 TABLET, FILM COATED in 1 BOTTLE (68788-4139-1)Jul 6, 2026
68788-4139-330 TABLET, FILM COATED in 1 BOTTLE (68788-4139-3)Jul 6, 2026
68788-4139-550 TABLET, FILM COATED in 1 BOTTLE (68788-4139-5)Jul 6, 2026
68788-4139-660 TABLET, FILM COATED in 1 BOTTLE (68788-4139-6)Jul 6, 2026
68788-4139-990 TABLET, FILM COATED in 1 BOTTLE (68788-4139-9)Jul 6, 2026

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