Drug recall D-0290-2021
Product
Famotidine Tablets USP 40mg, 1,000-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India, NDC 65862-860-99
Reason for recall
Presence of foreign tablets/capsules: Famotidine 20mg and ibuprofen 400mg tablets were found in a lot of famotidine 40mg.
Lots and codes
Lot #: P2000467, Exp 7/2022
Recall details
- Recalling firm
- Aurobindo Pharma USA Inc., East Windsor, NJ
- Quantity
- 1296 bottles
- Distribution
- TX, CA, GA, PA
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 20, 2021
- Terminated
- October 12, 2023
Related products
- Famotidine – drug information
- NDC 65862-860 Famotidine · Famotidine 40 mg/1 · Aurobindo Pharma Limited
- NDC 65862-859 Famotidine · Famotidine 20 mg/1 · Aurobindo Pharma Limited