Status
Terminated
Drug Enforcement D-1435-2012
Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets
Classification
Class II
Report Date
August 8, 2012
Termination Date
January 24, 2013
Product Information
- Product description
- Dr. Reddy's Ciprofloxacin Tablets, USP 500 mg*, 500 Tablets, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-127-05
- Product quantity
- 1656 bottles
- Reason for recall
- Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets
- Recall initiation reason
- —
- Initial firm notification
- Letter
- Distribution pattern
- Nationwide and Puerto Rico
Location & Firm
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Address
-
200 Somerset Corporate Blvd Fl 7th, N/A
United States - Voluntary / Mandated
- Voluntary: Firm initiated
- Status date
- —
Codes & Dates
- Recall number
- D-1435-2012
- Event ID
- 62591
- Recall initiation date
- April 9, 2012
- Center classification date
- July 31, 2012
- Code info
- C201293 Exp Date 08/2013
- More code info
- —