FDAClass IIINovember 11, 2020

Olanzapine Orally Disintegrating Tablets recall: Subpotent

Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by: Jubilant Generics, Ltd., Roorkee…

Why was Olanzapine Orally Disintegrating Tablets recalled?

Subpotent

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot # AE119001A, exp. date 01/2021

Product
Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by: Jubilant Generics, Ltd., Roorkee…
Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
Quantity
23,616 blister packs
Distribution
Product was distributed nationwide
Recall date
November 11, 2020
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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