Sun Pharmaceutical Industries Inc. recalls Nimodipine Capsules 30 mg, Rx Only, For Institutional Use Only, a) 30-count unit dose Capsules (5x6 blister cards per ca
Recalled July 17, 2013 · FDA recall D-687-2013 · Sun Pharmaceutical Industries
Hazard
Crystallization; crystallized nimodipine · FDA Class II
Units
46387 Cartons
Sold at
Nationwide and Puerto Rico
Description
Crystallization; crystallized nimodipine
Product
Nimodipine Capsules 30 mg, Rx Only, For Institutional Use Only, a) 30-count unit dose Capsules (5x6 blister cards per carton), NDC 57664-135-64, b) 100-count unit dose Capsules (25x4 blister cards per carton), NDC 57664-135-65, Distributed by: Caraco Pharmaceutical Laboratories, Ltd. Detroit, MI 48202 Affiliate of Sun Pharmaceutical Industries, Inc.
Manufacturer(s)
Sun Pharmaceutical Industries Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →