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=ANDA202354"
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
0143-9310-10 0143-9310 HUMAN PRESCRIPTION DRUG Etomidate Etomidate INJECTION INTRAVENOUS 20160225 N/A ANDA ANDA202354 Hikma Pharmaceuticals USA Inc. ETOMIDATE 2 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9310-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0143-9310-01)
0143-9311-10 0143-9311 HUMAN PRESCRIPTION DRUG Etomidate Etomidate INJECTION INTRAVENOUS 20160225 N/A ANDA ANDA202354 Hikma Pharmaceuticals USA Inc. ETOMIDATE 2 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9311-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0143-9311-01)
0143-9506-10 0143-9506 HUMAN PRESCRIPTION DRUG Etomidate Etomidate INJECTION INTRAVENOUS 20160225 N/A ANDA ANDA202354 Hikma Pharmaceuticals USA Inc. ETOMIDATE 2 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9506-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0143-9506-01)
0143-9507-10 0143-9507 HUMAN PRESCRIPTION DRUG Etomidate Etomidate INJECTION INTRAVENOUS 20160225 N/A ANDA ANDA202354 Hikma Pharmaceuticals USA Inc. ETOMIDATE 2 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9507-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0143-9507-01)
51662-1485-1 51662-1485 HUMAN PRESCRIPTION DRUG ETOMIDATE ETOMIDATE INJECTION INTRAVENOUS 20200111 N/A ANDA ANDA202354 HF Acquisition Co LLC, DBA HealthFirst ETOMIDATE 2 mg/mL 10 mL in 1 VIAL, SINGLE-DOSE (51662-1485-1)
72572-160-10 72572-160 HUMAN PRESCRIPTION DRUG Etomidate Etomidate INJECTION INTRAVENOUS 20220301 N/A ANDA ANDA202354 Civica, Inc. ETOMIDATE 2 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (72572-160-10) / 10 mL in 1 VIAL, SINGLE-DOSE (72572-160-01)
72572-161-10 72572-161 HUMAN PRESCRIPTION DRUG Etomidate Etomidate INJECTION INTRAVENOUS 20220301 N/A ANDA ANDA202354 Civica, Inc. ETOMIDATE 2 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (72572-161-10) / 20 mL in 1 VIAL, SINGLE-DOSE (72572-161-01)
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