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

Is NDC 67877-0544-88 recalled?

Cephalexin · 100 mL in 1 BOTTLE (67877-544-88)

Yes — this exact package was recalled

2 FDA recalls name the code 67877-0544-88 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.

2 of these recalls are still ongoing.

Active ingredient
Cephalexin
Strength
CEPHALEXIN 125 mg/5mL
Form
For Suspension · Oral
Labeler
Ascend Laboratories, LLC
Type
Human Prescription Drug
Product code
67877-0544

Recalls naming this package

Class II · Moderate risk

Cephalexin for Oral Suspension

Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.

Ongoing Impurity / degradation Ascend Laboratories, LLC NDC 67877-544-68 D-0469-2025
Class II · Moderate risk

Cephalexin for Oral Suspension

Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.

Ongoing Impurity / degradation Ascend Laboratories, LLC NDC 67877-544-88 D-0468-2025
Class II · Moderate risk

Cephalexin for Oral Suspension

Failed Impurity/Degradation Specifications: Unidentified impurities not complying with specifications were observed in various lots of Cephalexin FOS USP 125 mg/5 mL.

Terminated Impurity / degradation Ascend Laboratories LLC NDC 67877-544-88 D-0185-2021

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