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=ANDA076056"
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
55154-5370-0 55154-5370 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20120210 20260831 ANDA ANDA076056 Cardinal Health 107, LLC PRAVASTATIN SODIUM 40 mg/1 10 BLISTER PACK in 1 BAG (55154-5370-0) / 1 TABLET in 1 BLISTER PACK
0093-7201-10 0093-7201 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20060425 20261231 ANDA ANDA076056 Teva Pharmaceuticals USA, Inc. PRAVASTATIN SODIUM 20 mg/1 1000 TABLET in 1 BOTTLE (0093-7201-10)
0093-7201-98 0093-7201 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20060425 20260831 ANDA ANDA076056 Teva Pharmaceuticals USA, Inc. PRAVASTATIN SODIUM 20 mg/1 90 TABLET in 1 BOTTLE (0093-7201-98)
68071-3788-9 68071-3788 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20250203 N/A ANDA ANDA076056 NuCare Pharmaceuticals, Inc. PRAVASTATIN SODIUM 20 mg/1 90 TABLET in 1 BOTTLE (68071-3788-9)
70518-4408-0 70518-4408 HUMAN PRESCRIPTION DRUG Pravastatin sodium Pravastatin sodium TABLET ORAL 20250728 N/A ANDA ANDA076056 REMEDYREPACK INC. PRAVASTATIN SODIUM 20 mg/1 30 TABLET in 1 BLISTER PACK (70518-4408-0)
70518-4408-1 70518-4408 HUMAN PRESCRIPTION DRUG Pravastatin sodium Pravastatin sodium TABLET ORAL 20250824 N/A ANDA ANDA076056 REMEDYREPACK INC. PRAVASTATIN SODIUM 20 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-4408-1)
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