FDA Drug Recalls

Recalls / Class II

Class IID-0450-2017

Product

Flucanozole Tablets, USP, 100 mg, a) 30 count (NDC 55111-144-30) and b) 100 count (NDC 55111-144-01) bottles, Rx Only, Mfd. by: Dr. Reddy's Laboratories, Bachupally 500 090 India

Brand name
Fluconazole
Generic name
Fluconazole
Active ingredient
Fluconazole
Route
Oral
NDCs
55111-143, 55111-144, 55111-145, 55111-146
FDA application
ANDA076658
Affected lot / code info
a) 30 count C500224, exp 12/2016, C500846, exp 01/2017 b) 100 count C500224, exp 12/2016, exp 12/2016, C501608, exp 02/2017 and C503655, exp 04/2017

Why it was recalled

Failed Dissolution Specifications; 18 month stability time point

Recalling firm

Firm
Dr. Reddy's Laboratories, Inc.
Manufacturer
Dr. Reddy's Laboratories Limited
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
107 College Rd E, N/A, Princeton, New Jersey 08540-6623

Distribution

Quantity
a) 42,984 and b) 7,764 bottles
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-12-28
FDA classified
2017-01-30
Posted by FDA
2017-02-08
Terminated
2017-10-19
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0450-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: Fluconazole · FDA Drug Recalls