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
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)
71335-2885-1 71335-2885 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20251023 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2885-1)
68001-474-00 68001-474 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-00)
68001-474-03 68001-474 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-03)
29300-140-01 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/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-01)
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)
51655-365-52 51655-365 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20200529 N/A ANDA ANDA079163 Northwind Health Company, LLC DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-365-52)
70518-2626-2 70518-2626 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250806 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2626-2)
70518-4575-0 70518-4575 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20260217 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-4575-0)
72162-2460-1 72162-2460 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250221 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-1)
72162-2460-3 72162-2460 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250221 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-3)
72162-2460-5 72162-2460 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250221 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-5)
61919-249-30 61919-249 HUMAN PRESCRIPTION DRUG DIVALPROEX SODIUM divalproex sodium TABLET, DELAYED RELEASE ORAL 20220406 N/A ANDA ANDA079163 DirectRx DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-30)
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)
60687-879-61 60687-879 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250206 N/A ANDA ANDA079163 American Health Packaging DIVALPROEX SODIUM 500 mg/1 90 BLISTER PACK in 1 CARTON (60687-879-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-879-11)
71335-2124-1 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-1)
71335-2124-2 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-2)
71335-2124-3 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-3)
71335-2124-4 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-4)
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