FDAClass IIIJanuary 11, 2017

Temazepam Capsules USP recall

TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21

Why was Temazepam Capsules USP recalled?

Failed Stability Specifications

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?

T248H15A, Exp. 08/17

Product
TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21
Recalling firm
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
Quantity
1200 bottles
Distribution
Nationwide
Recall date
January 11, 2017
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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