NDC 68788-7529

Cephalexin 250 mg per 5 mL for suspension

On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Ascend Laboratories, LLC's NDC 67877-545.

Where the pills inside were made

Repackaging site

• Preferred Pharmaceuticals Inc., Anaheim, CA, United States · relabels it

Recalls

• Apr 12, 2021 · Class II · Preferred Pharmaceuticals, Inc.
  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
  Lots: Lot #: B1121W, Exp.Date: 04/2022
• Jan 22, 2021 · Class II · Ascend Laboratories LLC
  CGMP Deviations: Individual Unidentified impurities results of the product was found at higher side of the specification limit.
  Lots: Lot # 19144841, Exp 9/2021; 20141673 Exp 4/2022.
• Jan 22, 2021 · Class II · Ascend Laboratories LLC
  CGMP Deviations: Individual Unidentified impurities results of the product was found at higher side of the specification limit.
  Lots: Lot #: 19141869, 19141870, EXP 3/2021; 19142762, EXP 5/2021; 19143826, 19143923,19143941, 19143954 EXP 7/2021
• Dec 17, 2020 · Class II · Ascend Laboratories LLC
  Failed Impurity/Degradation Specifications
  Lots: 20141674, 20141675, 20141676, 20141677, 20141678,
• Dec 17, 2020 · Class II · Ascend Laboratories LLC
  Failed Impurity/Degradation Specifications
  Lots: 20141680, 20141681, 20141759

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Cephalexin: every company that makes it

Form

for suspension, oral

Strength

250 mg per 5 mL

Approval

ANDA ANDA210221

On the market since

Mar 28, 2019

Package NDCs

68788-7529-1 68788-7529-2

Official label

DailyMed (National Library of Medicine), updated Mar 25, 2026

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