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=ANDA210184"
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
70771-1365-5 70771-1365 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 30 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-5)
70771-1365-7 70771-1365 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 30 mg/1 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-7)
70771-1365-9 70771-1365 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 30 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-9)
70771-1366-0 70771-1366 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 60 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1366-0)
70771-1366-1 70771-1366 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 60 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1366-1)
70771-1366-4 70771-1366 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 60 mg/1 10 BLISTER PACK in 1 CARTON (70771-1366-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1366-7 70771-1366 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 60 mg/1 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1366-7)
70771-1366-9 70771-1366 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 60 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1366-9)
70771-1367-0 70771-1367 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 90 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1367-0)
70771-1365-4 70771-1365 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 30 mg/1 10 BLISTER PACK in 1 CARTON (70771-1365-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1365-1 70771-1365 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 30 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-1)
70771-1365-0 70771-1365 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 30 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-0)
70771-1367-1 70771-1367 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 90 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1367-1)
70771-1367-4 70771-1367 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 90 mg/1 10 BLISTER PACK in 1 CARTON (70771-1367-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1367-7 70771-1367 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 90 mg/1 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1367-7)
70771-1367-9 70771-1367 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Lifesciences Limited NIFEDIPINE 90 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1367-9)
68382-688-01 68382-688 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Pharmaceuticals (USA) Inc. NIFEDIPINE 30 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-01)
68382-688-77 68382-688 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Pharmaceuticals (USA) Inc. NIFEDIPINE 30 mg/1 10 BLISTER PACK in 1 CARTON (68382-688-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
68382-688-95 68382-688 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Pharmaceuticals (USA) Inc. NIFEDIPINE 30 mg/1 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-95)
68382-689-01 68382-689 HUMAN PRESCRIPTION DRUG NIFEDIPINE NIFEDIPINE TABLET, EXTENDED RELEASE ORAL 20180818 N/A ANDA ANDA210184 Zydus Pharmaceuticals (USA) Inc. NIFEDIPINE 60 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-689-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase