NDC 53746-137 – Ibuprofen

Ibuprofen 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC53746-137

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071935
Marketed since
January 5, 2009
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (6)

Package NDCDescriptionSince
53746-137-01100 TABLET in 1 BOTTLE (53746-137-01)Jan 5, 2009
53746-137-05500 TABLET in 1 BOTTLE (53746-137-05)Jan 5, 2009
53746-137-3030 TABLET in 1 BOTTLE (53746-137-30)Jan 5, 2009
53746-137-5050 TABLET in 1 BOTTLE (53746-137-50)Jan 5, 2009
53746-137-6060 TABLET in 1 BOTTLE (53746-137-60)Jan 5, 2009
53746-137-9090 TABLET in 1 BOTTLE (53746-137-90)Jan 5, 2009

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