PlainRecalls
FDA Drug Low Class III Terminated

VIRACEPT (R) (nelfinavir mesylate) Tablets, 625 mg, 120-count bottle, Rx only, Manufactured by: Agouron Pharmaceuticals, Inc. A Pfizer Company, Distributed by: ViV Healthcare Company, Research Triangle Park, NC 27709 NDC 63010-027-70

Reported: July 23, 2014 Initiated: July 8, 2014 #D-1443-2014

Product Description

VIRACEPT (R) (nelfinavir mesylate) Tablets, 625 mg, 120-count bottle, Rx only, Manufactured by: Agouron Pharmaceuticals, Inc. A Pfizer Company, Distributed by: ViV Healthcare Company, Research Triangle Park, NC 27709 NDC 63010-027-70

Reason for Recall

Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled with an incorrect expiry date 11/2016. The correct expiry date is 09/2016.

Details

Recalling Firm
Pfizer Inc.
Units Affected
1200 tablets
Distribution
Nationwide and Puerto Rico
Location
New York, NY

Frequently Asked Questions

What product was recalled?
VIRACEPT (R) (nelfinavir mesylate) Tablets, 625 mg, 120-count bottle, Rx only, Manufactured by: Agouron Pharmaceuticals, Inc. A Pfizer Company, Distributed by: ViV Healthcare Company, Research Triangle Park, NC 27709 NDC 63010-027-70. Recalled by Pfizer Inc.. Units affected: 1200 tablets.
Why was this product recalled?
Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled with an incorrect expiry date 11/2016. The correct expiry date is 09/2016.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 23, 2014. Severity: Low. Recall number: D-1443-2014.