FDAClass IIMarch 12, 2014

Alprazolam Extended-Release Tablets recall: Failed Dissolution

Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue…

Why was Alprazolam Extended-Release Tablets recalled?

Failed Dissolution Specifications: Product did not meet specification requirements for dissolution.

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 #: 57617531, Exp 03/14

Product
Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue…
Recalling firm
Actavis Elizabeth LLC
Quantity
5,148 bottles
Distribution
Nationwide
Recall date
March 12, 2014
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls