Drug recall D-0738-2022
Product
Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090, India, NDC 55111-399-90.
Reason for recall
Failed Dissolution Specifications; during long term stability testing.
Lots and codes
Lot# C2102911, Exp. 12/2023
Recall details
- Recalling firm
- Dr. Reddy's Laboratories, Inc., Princeton, NJ
- Quantity
- 7,703 bottles
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 23, 2022
- Terminated
- February 2, 2024
Related products
- Lansoprazole – drug information
- NDC 55111-398 Lansoprazole · Lansoprazole 15 mg/1 · Dr.Reddy's Laboratories Ltd.
- NDC 55111-399 Lansoprazole · Lansoprazole 30 mg/1 · Dr.Reddy's Laboratories Ltd.