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=ANDA204453"
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
67877-644-01 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-01)
67877-644-05 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-05)
67877-644-14 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 10 BLISTER PACK in 1 CARTON (67877-644-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-644-30 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-30)
67877-578-01 67877-578 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 45 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-578-01)
67877-578-05 67877-578 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 45 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-578-05)
67877-578-14 67877-578 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 45 mg/1 10 BLISTER PACK in 1 CARTON (67877-578-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-578-30 67877-578 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 45 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-578-30)
71335-2201-1 71335-2201 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230804 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2201-1)
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