PlainRecalls
FDA Drug Low Class III Terminated

Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC 63739-669-10

Reported: October 5, 2016 Initiated: September 15, 2016 #D-1527-2016

Product Description

Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC 63739-669-10

Reason for Recall

Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).

Details

Units Affected
3,492 unit cartons of 10 x 10 blister cards
Distribution
CO, IL, LA, OH
Location
Concord, NC

Frequently Asked Questions

What product was recalled?
Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC 63739-669-10. Recalled by Mckesson Packaging Services. Units affected: 3,492 unit cartons of 10 x 10 blister cards.
Why was this product recalled?
Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).
Which agency issued this recall?
This recall was issued by the FDA Drug on October 5, 2016. Severity: Low. Recall number: D-1527-2016.