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
29300-138-05 29300-138 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 125 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-05)
29300-138-10 29300-138 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 125 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10)
67046-1136-3 67046-1136 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20241111 N/A ANDA ANDA079163 Coupler LLC DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1136-3)
29300-139-01 29300-139 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-01)
29300-139-05 29300-139 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-05)
29300-139-10 29300-139 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 250 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-10)
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)
50090-2007-0 50090-2007 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20150918 N/A ANDA ANDA079163 A-S Medication Solutions DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-0)
50090-2007-1 50090-2007 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20170802 N/A ANDA ANDA079163 A-S Medication Solutions DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-1)
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)
71335-2862-1 71335-2862 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20251023 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2862-1)
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)
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)
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