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=ANDA212654"
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
11788-078-01 11788-078 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20251101 N/A ANDA ANDA212654 AiPing Pharmaceutical, Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (11788-078-01)
11788-078-10 11788-078 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20251101 N/A ANDA ANDA212654 AiPing Pharmaceutical, Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (11788-078-10)
11788-079-01 11788-079 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20251101 N/A ANDA ANDA212654 AiPing Pharmaceutical, Inc. AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (11788-079-01)
11788-079-10 11788-079 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20251101 N/A ANDA ANDA212654 AiPing Pharmaceutical, Inc. AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (11788-079-10)
11788-080-01 11788-080 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20251101 N/A ANDA ANDA212654 AiPing Pharmaceutical, Inc. AMITRIPTYLINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (11788-080-01)
11788-081-01 11788-081 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20251101 N/A ANDA ANDA212654 AiPing Pharmaceutical, Inc. AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (11788-081-01)
11788-082-01 11788-082 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20251101 N/A ANDA ANDA212654 AiPing Pharmaceutical, Inc. AMITRIPTYLINE HYDROCHLORIDE 150 mg/1 100 TABLET in 1 BOTTLE (11788-082-01)
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