Drug recall D-0312-2025
Product
Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-139-05; b) 1000-count bottles, NDC 62756-139-04; Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway, Halol-389 350, Gujarat, India.
Reason for recall
Cross Contamination
Lots and codes
Lot # a) HAD1712B, Exp. date 03/2025 b) HAD1712C, exp. date 03/2025
Recall details
- Recalling firm
- SUN PHARMACEUTICAL INDUSTRIES INC, Princeton, NJ
- Quantity
- 852 bottles
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 4, 2025
Related products
- Gabapentin – drug information
- NDC 62756-138 Gabapentin · Gabapentin 300 mg/1 · Sun Pharmaceutical Industries, Inc.
- NDC 62756-139 Gabapentin · Gabapentin 400 mg/1 · Sun Pharmaceutical Industries, Inc.
- NDC 62756-202 Gabapentin · Gabapentin 600 mg/1 · Sun Pharmaceutical Industries, Inc.
- NDC 62756-137 Gabapentin · Gabapentin 100 mg/1 · Sun Pharmaceutical Industries, Inc.
- NDC 62756-204 Gabapentin · Gabapentin 800 mg/1 · Sun Pharmaceutical Industries, Inc.