NDC 68788-8757 – Ibuprofen

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

Human Prescription Drug

Product NDC68788-8757

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 17, 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
68788-8757-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8757-1)Oct 17, 2024
68788-8757-220 TABLET, FILM COATED in 1 BOTTLE (68788-8757-2)Oct 17, 2024
68788-8757-330 TABLET, FILM COATED in 1 BOTTLE (68788-8757-3)Oct 17, 2024
68788-8757-414 TABLET, FILM COATED in 1 BOTTLE (68788-8757-4)Oct 17, 2024
68788-8757-550 TABLET, FILM COATED in 1 BOTTLE (68788-8757-5)Oct 17, 2024
68788-8757-660 TABLET, FILM COATED in 1 BOTTLE (68788-8757-6)Oct 17, 2024
68788-8757-721 TABLET, FILM COATED in 1 BOTTLE (68788-8757-7)Oct 17, 2024
68788-8757-8120 TABLET, FILM COATED in 1 BOTTLE (68788-8757-8)Oct 17, 2024
68788-8757-990 TABLET, FILM COATED in 1 BOTTLE (68788-8757-9)Oct 17, 2024

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