NDC 0093-4137 – Cefdinir

Cefdinir Monohydrate 250 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug 1 recall

Product NDC0093-4137

Product details

Brand name
Cefdinir
Generic name
Cefdinir
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA065332
Marketed since
May 8, 2007
Listing expires
December 31, 2026
Pharmacologic class
Cephalosporin Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Cefdinir →

Package NDC codes (2)

Package NDCDescriptionSince
0093-4137-6460 mL in 1 BOTTLE (0093-4137-64)May 8, 2007
0093-4137-73100 mL in 1 BOTTLE (0093-4137-73)May 8, 2007

Recalls mentioning this NDC

Other Cefdinir products