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=ANDA218404"
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
70756-658-10 70756-658 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20240229 N/A ANDA ANDA218404 Lifestar Pharma LLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-10) / 1 mL in 1 VIAL, SINGLE-DOSE
70756-658-25 70756-658 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20240229 N/A ANDA ANDA218404 Lifestar Pharma LLC NALOXONE HYDROCHLORIDE .4 mg/mL 25 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-25) / 1 mL in 1 VIAL, SINGLE-DOSE
70756-658-82 70756-658 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20240229 N/A ANDA ANDA218404 Lifestar Pharma LLC NALOXONE HYDROCHLORIDE .4 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-82) / 1 mL in 1 VIAL, SINGLE-DOSE
72603-590-10 72603-590 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20240701 N/A ANDA ANDA218404 NorthStar RxLLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (72603-590-10) / 1 mL in 1 VIAL, SINGLE-DOSE
72603-590-25 72603-590 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20240701 N/A ANDA ANDA218404 NorthStar RxLLC NALOXONE HYDROCHLORIDE .4 mg/mL 25 VIAL, SINGLE-DOSE in 1 CARTON (72603-590-25) / 1 mL in 1 VIAL, SINGLE-DOSE
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