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=ANDA214823"
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
51407-812-30 51407-812 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230531 N/A ANDA ANDA214823 Golden State Medical Supply, Inc. DOXEPIN HYDROCHLORIDE 6 mg/1 30 TABLET in 1 BOTTLE (51407-812-30)
72205-052-05 72205-052 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230405 N/A ANDA ANDA214823 Novadoz Pharmaceuticals LLC DOXEPIN HYDROCHLORIDE 3 mg/1 500 TABLET in 1 BOTTLE (72205-052-05)
72205-052-30 72205-052 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230405 N/A ANDA ANDA214823 Novadoz Pharmaceuticals LLC DOXEPIN HYDROCHLORIDE 3 mg/1 30 TABLET in 1 BOTTLE (72205-052-30)
72205-052-91 72205-052 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230405 N/A ANDA ANDA214823 Novadoz Pharmaceuticals LLC DOXEPIN HYDROCHLORIDE 3 mg/1 100 TABLET in 1 BOTTLE (72205-052-91)
72205-053-05 72205-053 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230405 N/A ANDA ANDA214823 Novadoz Pharmaceuticals LLC DOXEPIN HYDROCHLORIDE 6 mg/1 500 TABLET in 1 BOTTLE (72205-053-05)
72205-053-30 72205-053 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230405 N/A ANDA ANDA214823 Novadoz Pharmaceuticals LLC DOXEPIN HYDROCHLORIDE 6 mg/1 30 TABLET in 1 BOTTLE (72205-053-30)
72205-053-91 72205-053 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230405 N/A ANDA ANDA214823 Novadoz Pharmaceuticals LLC DOXEPIN HYDROCHLORIDE 6 mg/1 100 TABLET in 1 BOTTLE (72205-053-91)
51407-811-30 51407-811 HUMAN PRESCRIPTION DRUG Doxepin hydrochloride Doxepin hydrochloride TABLET ORAL 20230531 N/A ANDA ANDA214823 Golden State Medical Supply, Inc. DOXEPIN HYDROCHLORIDE 3 mg/1 30 TABLET in 1 BOTTLE (51407-811-30)
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