NDC 68788-9110 – Ibuprofen

Ibuprofen 400 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68788-9110

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075682
Marketed since
November 20, 2008
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (8)

Package NDCDescriptionSince
68788-9110-1100 TABLET in 1 BOTTLE (68788-9110-1)Nov 20, 2008
68788-9110-220 TABLET in 1 BOTTLE (68788-9110-2)Nov 20, 2008
68788-9110-330 TABLET in 1 BOTTLE (68788-9110-3)Nov 20, 2008
68788-9110-550 TABLET in 1 BOTTLE (68788-9110-5)Nov 20, 2008
68788-9110-660 TABLET in 1 BOTTLE (68788-9110-6)Nov 20, 2008
68788-9110-721 TABLET in 1 BOTTLE (68788-9110-7)Nov 20, 2008
68788-9110-8120 TABLET in 1 BOTTLE (68788-9110-8)Nov 20, 2008
68788-9110-990 TABLET in 1 BOTTLE (68788-9110-9)Nov 20, 2008

Recalls mentioning this NDC

Other Ibuprofen products