FDAClass IIIJuly 6, 2016

Benzphetamine Hydrochloride Tablets recall

Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03

Why was Benzphetamine Hydrochloride Tablets recalled?

Discoloration: presence of scuffing marks on tablets.

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 #: 12825 A, 12937A, Exp 8/18

Product
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
Recalling firm
KVK-Tech, Inc.
Quantity
9360 bottles of lot # 12825A and 7284 bottles of lot # 12937A
Distribution
Nationwide
Recall date
July 6, 2016
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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