NDC 51672-1385 – Ibuprofen

Ibuprofen 100 mg/5mL · Suspension · Oral

Human Prescription Drug 2 recalls

Product NDC51672-1385

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA209204
Marketed since
June 23, 2017
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (2)

Package NDCDescriptionSince
51672-1385-81 BOTTLE in 1 CARTON (51672-1385-8) / 118 mL in 1 BOTTLEJun 23, 2017
51672-1385-9473 mL in 1 BOTTLE (51672-1385-9)Jun 23, 2017

Recalls mentioning this NDC

Other Ibuprofen products