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=ANDA210614"
符合检索条件的记录共 56 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
50090-6450-2 50090-6450 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20230427 N/A ANDA ANDA210614 A-S Medication Solutions NIFEDIPINE 90 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6450-2)
71335-2132-1 71335-2132 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20220727 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 90 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-1)
71335-2132-2 71335-2132 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20220727 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 90 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-2)
71335-2132-3 71335-2132 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20220727 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 90 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-3)
71335-2132-4 71335-2132 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20220727 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 90 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-4)
71335-2132-5 71335-2132 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20220727 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 90 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-5)
51655-593-26 51655-593 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20230103 N/A ANDA ANDA210614 Northwind Health Company, LLC NIFEDIPINE 30 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-593-26)
71335-1550-1 71335-1550 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20201204 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 30 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1550-1)
71335-1550-2 71335-1550 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20221013 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 30 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1550-2)
71335-1550-3 71335-1550 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20200325 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 30 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1550-3)
71335-1550-4 71335-1550 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20200806 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 30 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1550-4)
71335-1550-5 71335-1550 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20221013 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 30 mg/1 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1550-5)
71335-1550-6 71335-1550 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20221013 N/A ANDA ANDA210614 Bryant Ranch Prepack NIFEDIPINE 30 mg/1 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1550-6)
50742-261-01 50742-261 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190312 N/A ANDA ANDA210614 Ingenus Pharmaceuticals, LLC NIFEDIPINE 60 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-261-01)
50742-261-03 50742-261 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190312 N/A ANDA ANDA210614 Ingenus Pharmaceuticals, LLC NIFEDIPINE 60 mg/1 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-261-03)
50742-261-30 50742-261 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190312 N/A ANDA ANDA210614 Ingenus Pharmaceuticals, LLC NIFEDIPINE 60 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-261-30)
55154-4157-0 55154-4157 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20220512 N/A ANDA ANDA210614 Cardinal Health 107, LLC NIFEDIPINE 60 mg/1 10 BLISTER PACK in 1 BAG (55154-4157-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70518-3520-0 70518-3520 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, EXTENDED RELEASE ORAL 20220914 N/A ANDA ANDA210614 REMEDYREPACK INC. NIFEDIPINE 60 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3520-0)
0904-7081-06 0904-7081 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190312 N/A ANDA ANDA210614 Major Pharmaceuticals NIFEDIPINE 60 mg/1 50 BLISTER PACK in 1 CARTON (0904-7081-06) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
0904-7081-61 0904-7081 HUMAN PRESCRIPTION DRUG Nifedipine nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190312 N/A ANDA ANDA210614 Major Pharmaceuticals NIFEDIPINE 60 mg/1 100 BLISTER PACK in 1 CARTON (0904-7081-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase