美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=NALMEFENE HYDROCHLORIDE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
NALMEFENE HYDROCHLORIDE 212955 001 ANDA NALMEFENE HYDROCHLORIDE SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS EQ 2MG BASE/2ML (EQ 1MG BASE/ML) No Yes 2022/02/08 2022/02/08 PURDUE PHARMA LP Prescription
NALMEFENE HYDROCHLORIDE 216007 001 ANDA NALMEFENE HYDROCHLORIDE SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) No Yes 2023/11/15 2023/11/15 CHENGDU SHUODE Prescription
NALMEFENE HYDROCHLORIDE 216007 002 ANDA NALMEFENE HYDROCHLORIDE SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS EQ 2MG BASE/2ML (EQ 1MG BASE/ML) No No 2023/11/15 2023/11/15 CHENGDU SHUODE Prescription
NALMEFENE HYDROCHLORIDE 216007 003 ANDA NALMEFENE HYDROCHLORIDE SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS 2MG BASE/2ML (EQ 1MGBASE/ML) No No 2023/11/15 -- CHENGDU SHUODE Prescription
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