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

Is NDC 68788-7529-01 recalled?

Cephalexin · 100 mL in 1 BOTTLE (68788-7529-1)

Yes — this exact package was recalled

1 FDA recall names the code 68788-7529-01 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.

1 of these recalls is still ongoing.

Active ingredient
Cephalexin
Strength
CEPHALEXIN 250 mg/5mL
Form
For Suspension · Oral
Labeler
Preferred Pharmaceuticals, Inc.
Type
Human Prescription Drug
Product code
68788-7529

Recalls naming this package

Class II ยท Moderate risk

Cephalexin for Oral Suspension

Failed Impurities/degradation specifications: Repackager recall due to Out of Specification detected by manufacturer for Individual Unidentified Impurity found during related substance test analysis of Cephalexin

Ongoing Impurity / degradation Preferred Pharmaceuticals, Inc. D-0342-2021

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