NDC 0093-4175 – Cephalexin

Cephalexin 125 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug 3 recalls

Product NDC0093-4175

Product details

Brand name
Cephalexin
Generic name
Cephalexin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA062703
Marketed since
September 30, 1990
Listing expires
December 31, 2026
Pharmacologic class
Cephalosporin Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Cephalexin →

Package NDC codes (2)

Package NDCDescriptionSince
0093-4175-73100 mL in 1 BOTTLE (0093-4175-73)Sep 30, 1990
0093-4175-74200 mL in 1 BOTTLE (0093-4175-74)Sep 30, 1990

Recalls mentioning this NDC

Other Cephalexin products