美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA078919"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
70518-2527-0 70518-2527 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20200106 N/A ANDA ANDA078919 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 100 POUCH in 1 BOX (70518-2527-0) / 1 CAPSULE, COATED PELLETS in 1 POUCH (70518-2527-1)
70518-1749-1 70518-1749 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20181227 N/A ANDA ANDA078919 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 100 POUCH in 1 BOX (70518-1749-1) / 1 CAPSULE, COATED PELLETS in 1 POUCH (70518-1749-0)
68382-106-77 68382-106 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20090127 N/A ANDA ANDA078919 Zydus Pharmaceuticals USA Inc. DIVALPROEX SODIUM 125 mg/1 100 BLISTER PACK in 1 CARTON (68382-106-77) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68382-106-30)
68382-106-10 68382-106 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20090127 N/A ANDA ANDA078919 Zydus Pharmaceuticals USA Inc. DIVALPROEX SODIUM 125 mg/1 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-10)
68382-106-01 68382-106 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20090127 N/A ANDA ANDA078919 Zydus Pharmaceuticals USA Inc. DIVALPROEX SODIUM 125 mg/1 100 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-01)
65841-639-10 65841-639 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20090127 N/A ANDA ANDA078919 Zydus Lifesciences Limited DIVALPROEX SODIUM 125 mg/1 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (65841-639-10)
68084-313-01 68084-313 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium CAPSULE, COATED PELLETS ORAL 20090318 N/A ANDA ANDA078919 American Health Packaging DIVALPROEX SODIUM 125 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-313-01) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)
68084-313-65 68084-313 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium CAPSULE, COATED PELLETS ORAL 20240526 N/A ANDA ANDA078919 American Health Packaging DIVALPROEX SODIUM 125 mg/1 50 BLISTER PACK in 1 CARTON (68084-313-65) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)
50268-258-13 50268-258 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20160714 N/A ANDA ANDA078919 AvPAK DIVALPROEX SODIUM 125 mg/1 30 BLISTER PACK in 1 BOX (50268-258-13) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (50268-258-11)
65841-639-30 65841-639 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20090127 N/A ANDA ANDA078919 Zydus Lifesciences Limited DIVALPROEX SODIUM 125 mg/1 10 BLISTER PACK in 1 CARTON (65841-639-30) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK
65841-639-01 65841-639 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium CAPSULE, COATED PELLETS ORAL 20090127 N/A ANDA ANDA078919 Zydus Lifesciences Limited DIVALPROEX SODIUM 125 mg/1 100 CAPSULE, COATED PELLETS in 1 BOTTLE (65841-639-01)
55154-4759-0 55154-4759 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium CAPSULE, COATED PELLETS ORAL 20090318 N/A ANDA ANDA078919 Cardinal Health 107, LLC DIVALPROEX SODIUM 125 mg/1 10 BLISTER PACK in 1 BAG (55154-4759-0) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK
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