Class II · Moderate risk
Cephalexin for Oral Suspension
CGMP Deviations: Individual Unidentified impurities results of the product was found at higher side of the specification limit.
National Drug Code
Is NDC 67877-0545-88 recalled?
Cephalexin · 100 mL in 1 BOTTLE (67877-545-88)
Yes — this exact package was recalled
2 FDA recalls name the code 67877-0545-88 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.
- Active ingredient
- Cephalexin
- Strength
- CEPHALEXIN 250 mg/5mL
- Form
- For Suspension · Oral
- Labeler
- Ascend Laboratories, LLC
- Type
- Human Prescription Drug
- Product code
- 67877-0545
Recalls naming this package
Class II · Moderate risk
Cephalexin for Oral Suspension
CGMP Deviations: Individual Unidentified impurities results of the product was found at higher side of the specification limit.
Class II · Moderate risk
Ascend Laboratories
Failed Impurity/Degradation Specifications
Class II · Moderate risk
Ascend Laboratories
Failed Impurity/Degradation Specifications
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
- 67877-0544 Cephalexin 3
- 67877-0590 Metoprolol Succinate 3
- 67877-0446 Olmesartan Medoxomil 2
- 67877-0474 Dabigatran Etexilate 2
- 67877-0475 Dabigatran Etexilate 2
- 67877-0501 Amlodipine and olmesartan Medoxomil 2
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