NDC 68788-8710 – Ibuprofen

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

Human Prescription Drug

Product NDC68788-8710

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078329
Marketed since
July 5, 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
68788-8710-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8710-1)Jul 5, 2024
68788-8710-220 TABLET, FILM COATED in 1 BOTTLE (68788-8710-2)Jul 5, 2024
68788-8710-330 TABLET, FILM COATED in 1 BOTTLE (68788-8710-3)Jul 5, 2024
68788-8710-414 TABLET, FILM COATED in 1 BOTTLE (68788-8710-4)Jul 5, 2024
68788-8710-550 TABLET, FILM COATED in 1 BOTTLE (68788-8710-5)Jul 5, 2024
68788-8710-660 TABLET, FILM COATED in 1 BOTTLE (68788-8710-6)Jul 5, 2024
68788-8710-721 TABLET, FILM COATED in 1 BOTTLE (68788-8710-7)Jul 5, 2024
68788-8710-8120 TABLET, FILM COATED in 1 BOTTLE (68788-8710-8)Jul 5, 2024
68788-8710-990 TABLET, FILM COATED in 1 BOTTLE (68788-8710-9)Jul 5, 2024

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