NDC 55111-684 – Ibu

Ibuprofen 800 mg/1 · Tablet · Oral

Human Prescription Drug 5 recalls

Product NDC55111-684

Product details

Brand name
Ibu
Generic name
Ibuprofen
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075682
Marketed since
November 20, 2008
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibu →

Package NDC codes (6)

Package NDCDescriptionSince
55111-684-01100 TABLET in 1 BOTTLE (55111-684-01)Nov 20, 2008
55111-684-05500 TABLET in 1 BOTTLE (55111-684-05)Nov 20, 2008
55111-684-0990 TABLET in 1 BOTTLE (55111-684-09)Nov 20, 2008
55111-684-3030 TABLET in 1 BOTTLE (55111-684-30)Nov 20, 2008
55111-684-5050 TABLET in 1 BOTTLE (55111-684-50)Nov 20, 2008
55111-684-6060 TABLET in 1 BOTTLE (55111-684-60)Nov 20, 2008

Recalls mentioning this NDC

Other Ibu products