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=ANDA040712"
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
68071-4686-1 68071-4686 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20181231 N/A ANDA ANDA040712 NuCare Pharmaceuticals,Inc. PROMETHAZINE HYDROCHLORIDE 25 mg/1 10 TABLET in 1 BOTTLE (68071-4686-1)
10702-004-01 10702-004 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20060731 N/A ANDA ANDA040712 KVK-Tech, Inc. PROMETHAZINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (10702-004-01)
10702-004-10 10702-004 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20060731 N/A ANDA ANDA040712 KVK-Tech, Inc. PROMETHAZINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (10702-004-10)
71335-0989-1 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 12 TABLET in 1 BOTTLE (71335-0989-1)
71335-0989-2 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 4 TABLET in 1 BOTTLE (71335-0989-2)
71335-0989-3 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 2 TABLET in 1 BOTTLE (71335-0989-3)
71335-0989-5 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 6 TABLET in 1 BOTTLE (71335-0989-5)
71335-0989-6 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20211201 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 10 TABLET in 1 BOTTLE (71335-0989-6)
71335-0989-7 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 40 TABLET in 1 BOTTLE (71335-0989-7)
71335-0989-8 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20240709 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 20 TABLET in 1 BOTTLE (71335-0989-8)
71335-0989-9 71335-0989 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20181030 N/A ANDA ANDA040712 Bryant Ranch Prepack PROMETHAZINE HYDROCHLORIDE 12.5 mg/1 60 TABLET in 1 BOTTLE (71335-0989-9)
50090-4608-0 50090-4608 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20191015 N/A ANDA ANDA040712 A-S Medication Solutions PROMETHAZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (50090-4608-0)
50090-4750-0 50090-4750 HUMAN PRESCRIPTION DRUG PROMETHAZINE HYDROCHLORIDE promethazine hydrochloride TABLET ORAL 20191122 N/A ANDA ANDA040712 A-S Medication Solutions PROMETHAZINE HYDROCHLORIDE 25 mg/1 12 TABLET in 1 BOTTLE (50090-4750-0)
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