US Drug Recall Register
Class III · Low risk Terminated Initiated Oct 26, 2020 (6 years ago)

Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack…

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

Why it was recalled

Subpotent

What was recalled

Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by: Jubilant Generics, Ltd., Roorkee, India, Marketed by: Jubilant Cardista Pharmaceuticals, Inc., Salisbury, MD NDC 59746-0306-32

Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
NDC code
59746-0306-32
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0066-2021

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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