PlainRecalls
FDA Drug Moderate Class II Terminated

RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10

Reported: March 14, 2018 Initiated: February 26, 2018 #D-0914-2018

Product Description

RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10

Reason for Recall

Failed Stability Specifications

Details

Units Affected
17,192 cartons (1,719,200 tablets)
Distribution
Nationwide
Location
Concord, NC

Frequently Asked Questions

What product was recalled?
RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10. Recalled by Mckesson Packaging Services. Units affected: 17,192 cartons (1,719,200 tablets).
Why was this product recalled?
Failed Stability Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on March 14, 2018. Severity: Moderate. Recall number: D-0914-2018.