Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 68180-0723-04 recalled?

Cefdinir · 60 mL in 1 BOTTLE (68180-723-04)

Yes — this exact package was recalled

2 FDA recalls name the code 68180-0723-04 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Cefdinir
Strength
CEFDINIR 250 mg/5mL
Form
Powder, for Suspension · Oral
Labeler
Lupin Pharmaceuticals, Inc.
Type
Human Prescription Drug
Product code
68180-0723

Recalls naming this package

Class II · Moderate risk

Cefdinir for Oral Suspension USP

CGMP Deviations: Product complaints received indicating reconstituted suspension was observed to be thick.

Terminated cGMP deviation Lupin Pharmaceuticals Inc. NDC 68180-723-20 D-0376-2019

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler