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=ANDA079163"
符合检索条件的记录共 50 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
29300-140-05 29300-140 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-05)
29300-140-10 29300-140 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 500 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-10)
63187-742-30 63187-742 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-30)
63187-742-60 63187-742 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60)
63187-742-90 63187-742 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 250 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-90)
63187-743-30 63187-743 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-30)
63187-743-60 63187-743 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-60)
63187-743-90 63187-743 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-90)
68788-7183-3 68788-7183 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180717 N/A ANDA ANDA079163 Preferred Pharmaceuticals Inc. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-3)
68788-7183-6 68788-7183 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180717 N/A ANDA ANDA079163 Preferred Pharmaceuticals Inc. DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-6)
68788-7183-9 68788-7183 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180717 N/A ANDA ANDA079163 Preferred Pharmaceuticals Inc. DIVALPROEX SODIUM 250 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-9)
61919-249-60 61919-249 HUMAN PRESCRIPTION DRUG DIVALPROEX SODIUM divalproex sodium TABLET, DELAYED RELEASE ORAL 20220406 N/A ANDA ANDA079163 DirectRx DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60)
70518-3620-0 70518-3620 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230121 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 100 POUCH in 1 BOX (70518-3620-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3620-1)
70518-3620-2 70518-3620 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230131 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3620-2)
70518-3620-3 70518-3620 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230203 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3620-3)
70518-3620-4 70518-3620 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230313 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3620-4)
68001-472-00 68001-472 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 125 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-00)
68001-472-03 68001-472 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 125 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03)
68001-473-00 68001-473 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-00)
68001-473-03 68001-473 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-03)
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