PlainRecalls
FDA Drug Moderate Class II Terminated

Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC 0185-0341-01,

Reported: January 8, 2014 Initiated: October 11, 2013 #D-393-2014

Product Description

Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC 0185-0341-01,

Reason for Recall

Subpotent; Hydrochlorothiazide at the 9 month time point.

Details

Recalling Firm
Sandoz Inc
Units Affected
2,491 bottles of 100 tablets each
Distribution
Nationwide
Location
Wilson, NC

Frequently Asked Questions

What product was recalled?
Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC 0185-0341-01,. Recalled by Sandoz Inc. Units affected: 2,491 bottles of 100 tablets each.
Why was this product recalled?
Subpotent; Hydrochlorothiazide at the 9 month time point.
Which agency issued this recall?
This recall was issued by the FDA Drug on January 8, 2014. Severity: Moderate. Recall number: D-393-2014.