Drug recall D-1434-2012
Product
Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-340-05
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.
Lots and codes
C201293 Exp Date 08/2013
Recall details
- Recalling firm
- Dr. Reddy's Laboratories, Inc., Bridgewater, NJ
- Quantity
- 1656 bottles
- Distribution
- Nationwide and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 9, 2012
- Terminated
- January 24, 2013
Related products
- Amlodipine Besylate and Benazepril Hydrochloride – drug information
- NDC 55111-339 Amlodipine Besylate and Benazepril Hydrochloride · Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 10 mg/1 · Dr.Reddy's Laboratories Limited
- NDC 55111-340 Amlodipine Besylate and Benazepril Hydrochloride · Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 20 mg/1 · Dr.Reddy's Laboratories Limited
- NDC 55111-341 Amlodipine Besylate and Benazepril Hydrochloride · Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 20… · Dr.Reddy's Laboratories Limited
- NDC 55111-338 Amlodipine Besylate and Benazepril Hydrochloride · Amlodipine Besylate 2.5 mg/1; Benazepril Hydrochloride 10… · Dr.Reddy's Laboratories Limited