NDC 68788-8754 – Ibuprofen

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

Human Prescription Drug

Product NDC68788-8754

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 14, 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 (9)

Package NDCDescriptionSince
68788-8754-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8754-1)Oct 14, 2024
68788-8754-220 TABLET, FILM COATED in 1 BOTTLE (68788-8754-2)Oct 14, 2024
68788-8754-330 TABLET, FILM COATED in 1 BOTTLE (68788-8754-3)Oct 14, 2024
68788-8754-414 TABLET, FILM COATED in 1 BOTTLE (68788-8754-4)Oct 14, 2024
68788-8754-550 TABLET, FILM COATED in 1 BOTTLE (68788-8754-5)Oct 14, 2024
68788-8754-660 TABLET, FILM COATED in 1 BOTTLE (68788-8754-6)Oct 14, 2024
68788-8754-721 TABLET, FILM COATED in 1 BOTTLE (68788-8754-7)Oct 14, 2024
68788-8754-8120 TABLET, FILM COATED in 1 BOTTLE (68788-8754-8)Oct 14, 2024
68788-8754-990 TABLET, FILM COATED in 1 BOTTLE (68788-8754-9)Oct 14, 2024

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