FlaggedRx← Medication recall checkHome
Class III · Lower riskActive recall

Verapamil Hydrochloride

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot L300269, Exp Date 07/31/2025
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Cross contamination with other products.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byZydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534, Vial foreign manufacturer
Brand nameVERAPAMIL HYDROCHLORIDE
Generic nameVERAPAMIL HYDROCHLORIDE
Active ingredient(s)VERAPAMIL HYDROCHLORIDE
Distributed by / forZydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534, Vial
NDC70710-1644-1
Show the full FDA record
Full product labelVerapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534, Vial NDC: 70710-1644-1, Carton NDC: 70710-1644-5.
Recalling firmZydus Pharmaceuticals (USA) Inc
DistributionNationwide in the USA
Quantity8020 vials
Recall initiated2024-07-02
Report date2024-07-17
Recall completed
Recall numberD-0593-2024
ClassificationClass III
FDA statusOngoing
Origin on filePennington NJ United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.