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=ANDA212300"
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
0641-6205-10 0641-6205 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20220610 N/A ANDA ANDA212300 Hikma Pharmaceuticals USA Inc. NALOXONE HYDROCHLORIDE 1 mg/mL 10 SYRINGE in 1 CARTON (0641-6205-10) / 2 mL in 1 SYRINGE (0641-6205-01)
0641-6193-10 0641-6193 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20250831 N/A ANDA ANDA212300 Hikma Pharmaceuticals USA Inc. NALOXONE HYDROCHLORIDE .4 mg/mL 10 SYRINGE in 1 CARTON (0641-6193-10) / 1 mL in 1 SYRINGE (0641-6193-01)
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