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=ANDA090284"
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
69097-844-02 69097-844 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride extended release Alfuzosin Hydrochloride TABLET ORAL 20160630 N/A ANDA ANDA090284 Cipla USA Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (69097-844-02)
69097-844-05 69097-844 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride extended release Alfuzosin Hydrochloride TABLET ORAL 20160630 N/A ANDA ANDA090284 Cipla USA Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (69097-844-05)
69097-844-07 69097-844 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride extended release Alfuzosin Hydrochloride TABLET ORAL 20160630 N/A ANDA ANDA090284 Cipla USA Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (69097-844-07)
69097-844-12 69097-844 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride extended release Alfuzosin Hydrochloride TABLET ORAL 20160630 N/A ANDA ANDA090284 Cipla USA Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 500 TABLET in 1 BOTTLE (69097-844-12)
76282-302-01 76282-302 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20121002 N/A ANDA ANDA090284 Exelan Pharmaceuticals Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-01)
76282-302-05 76282-302 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20121002 N/A ANDA ANDA090284 Exelan Pharmaceuticals Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-05)
76282-302-10 76282-302 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20121002 N/A ANDA ANDA090284 Exelan Pharmaceuticals Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-10)
76282-302-12 76282-302 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20221201 N/A ANDA ANDA090284 Exelan Pharmaceuticals Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-12)
76282-302-90 76282-302 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20190101 N/A ANDA ANDA090284 Exelan Pharmaceuticals Inc. ALFUZOSIN HYDROCHLORIDE 10 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-90)
43353-945-16 43353-945 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20140522 N/A ANDA ANDA090284 Aphena Pharma Solutions - Tennessee, LLC ALFUZOSIN HYDROCHLORIDE 10 mg/1 6000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-945-16)
43353-945-30 43353-945 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20150402 N/A ANDA ANDA090284 Aphena Pharma Solutions - Tennessee, LLC ALFUZOSIN HYDROCHLORIDE 10 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-945-30)
43353-945-60 43353-945 HUMAN PRESCRIPTION DRUG Alfuzosin hydrochloride Alfuzosin hydrochloride TABLET, EXTENDED RELEASE ORAL 20150402 N/A ANDA ANDA090284 Aphena Pharma Solutions - Tennessee, LLC ALFUZOSIN HYDROCHLORIDE 10 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-945-60)
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