NDC 68180-723 – Cefdinir

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

Human Prescription Drug 10 recalls

Product NDC68180-723

Product details

Brand name
Cefdinir
Generic name
Cefdinir
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA065259
Marketed since
May 7, 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
68180-723-0460 mL in 1 BOTTLE (68180-723-04)May 22, 2020
68180-723-05100 mL in 1 BOTTLE (68180-723-05)May 22, 2020

Recalls mentioning this NDC

Other Cefdinir products