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=ANDA216920"
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
0641-6261-01 0641-6261 HUMAN PRESCRIPTION DRUG Sodium Acetate Sodium Acetate INJECTION INTRAVENOUS 20240520 N/A ANDA ANDA216920 Hikma Pharmaceuticals USA Inc. SODIUM ACETATE ANHYDROUS 164 mg/mL 1 VIAL in 1 CARTON (0641-6261-01) / 20 mL in 1 VIAL
0641-6262-01 0641-6262 HUMAN PRESCRIPTION DRUG Sodium Acetate Sodium Acetate INJECTION INTRAVENOUS 20240520 N/A ANDA ANDA216920 Hikma Pharmaceuticals USA Inc. SODIUM ACETATE ANHYDROUS 164 mg/mL 1 VIAL in 1 CARTON (0641-6262-01) / 50 mL in 1 VIAL
0641-6263-10 0641-6263 HUMAN PRESCRIPTION DRUG Sodium Acetate Sodium Acetate INJECTION INTRAVENOUS 20240520 N/A ANDA ANDA216920 Hikma Pharmaceuticals USA Inc. SODIUM ACETATE ANHYDROUS 164 mg/mL 10 VIAL in 1 CARTON (0641-6263-10) / 100 mL in 1 VIAL (0641-6263-01)
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