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

FDA recall notice · announced July 6, 2016 · Kvk-tech

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

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

Reason for recall

Discoloration: presence of scuffing marks on tablets.

Notes

Distribution: Nationwide
Lot/code information: Lot #: 12825 A, 12937A, Exp 8/18
Quantity: 9360 bottles of lot # 12825A and 7284 bottles of lot # 12937A
Status: Terminated
Products in this recall event:
- Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03 (D-1057-2016)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.