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=ANDA207176"
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
10702-055-01 10702-055 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Homatropine Methylbromide Hydrocodone Bitartrate and Homatropine Methylbromide TABLET ORAL 20170807 N/A ANDA ANDA207176 KVK-Tech, Inc. HOMATROPINE METHYLBROMIDE; HYDROCODONE BITARTRATE 1.5 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE (10702-055-01)
10702-055-03 10702-055 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Homatropine Methylbromide Hydrocodone Bitartrate and Homatropine Methylbromide TABLET ORAL 20170807 N/A ANDA ANDA207176 KVK-Tech, Inc. HOMATROPINE METHYLBROMIDE; HYDROCODONE BITARTRATE 1.5 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE (10702-055-03)
10702-055-09 10702-055 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Homatropine Methylbromide Hydrocodone Bitartrate and Homatropine Methylbromide TABLET ORAL 20170807 N/A ANDA ANDA207176 KVK-Tech, Inc. HOMATROPINE METHYLBROMIDE; HYDROCODONE BITARTRATE 1.5 mg/1; 5 mg/1 90 TABLET in 1 BOTTLE (10702-055-09)
10702-055-10 10702-055 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Homatropine Methylbromide Hydrocodone Bitartrate and Homatropine Methylbromide TABLET ORAL 20170807 N/A ANDA ANDA207176 KVK-Tech, Inc. HOMATROPINE METHYLBROMIDE; HYDROCODONE BITARTRATE 1.5 mg/1; 5 mg/1 1000 TABLET in 1 BOTTLE (10702-055-10)
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