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=ANDA084176"
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
63739-213-10 63739-213 HUMAN PRESCRIPTION DRUG Promethazine Hydrochloride Promethazine Hydrochloride TABLET ORAL 19751219 20240930 ANDA ANDA084176 McKesson Corporation dba SKY Packaging PROMETHAZINE HYDROCHLORIDE 25 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-213-10) / 10 TABLET in 1 BLISTER PACK
55154-8080-0 55154-8080 HUMAN PRESCRIPTION DRUG Promethazine Hydrochloride Promethazine Hydrochloride TABLET ORAL 20150315 N/A ANDA ANDA084176 Cardinal Health 107, LLC PROMETHAZINE HYDROCHLORIDE 25 mg/1 1 BLISTER PACK in 1 BAG (55154-8080-0) / 10 TABLET in 1 BLISTER PACK
0781-1830-10 0781-1830 HUMAN PRESCRIPTION DRUG Promethazine Hydrochloride Promethazine Hydrochloride TABLET ORAL 19751219 20240930 ANDA ANDA084176 Sandoz Inc PROMETHAZINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (0781-1830-10)
0781-1830-01 0781-1830 HUMAN PRESCRIPTION DRUG Promethazine Hydrochloride Promethazine Hydrochloride TABLET ORAL 19751219 20240430 ANDA ANDA084176 Sandoz Inc PROMETHAZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (0781-1830-01)
0904-6461-61 0904-6461 HUMAN PRESCRIPTION DRUG Promethazine Hydrochloride Promethazine Hydrochloride TABLET ORAL 20150315 N/A ANDA ANDA084176 Major Pharmaceuticals PROMETHAZINE HYDROCHLORIDE 25 mg/1 100 BLISTER PACK in 1 CARTON (0904-6461-61) / 1 TABLET in 1 BLISTER PACK
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