US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 14, 2018 (8 years ago)

Valsartan Tablets USP, 40 mg, 30-count bottle, Rx only, Manufactured by: Jubilant…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.

What was recalled

Valsartan Tablets USP, 40 mg, 30-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd Roorkee 0247661 India, Marketed by: Jubilant Cardista Pharmaceuticals Inc. Salisbury, MD 21801, USA, NDC 59746-360-30

Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
NDC code
59746-360-30
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1103-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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