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SUN PHARMACEUTICAL INDUSTRIES INC recalls Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-139-05; b) 1000-count bottles, NDC

Recalled April 16, 2025 · FDA recall D-0312-2025 · SUN PHARMACEUTICAL INDUSTRIES

Hazard
Cross Contamination · FDA Class III
Units
852 bottles
Sold at
Nationwide in the USA

Description

Cross Contamination

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.
Manufacturer(s)
SUN PHARMACEUTICAL INDUSTRIES INC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

SUN PHARMACEUTICAL INDUSTRIES INC recalls Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-139-05; b) 1000-count bottles, NDC | RecallWatchUSA