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=ANDA090747"
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
0517-0720-01 0517-0720 HUMAN PRESCRIPTION DRUG Betamethasone Sodium Phosphate and Betamethasone Acetate Betamethasone Sodium Phosphate and Betamethasone Acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR 20100428 N/A ANDA ANDA090747 American Regent, Inc. BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE 3 mg/mL; 3 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0720-01) / 5 mL in 1 VIAL, MULTI-DOSE
0517-0799-01 0517-0799 HUMAN PRESCRIPTION DRUG Betamethasone Sodium Phosphate and Betamethasone Acetate Betamethasone Sodium Phosphate and Betamethasone Acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR 20191101 N/A ANDA ANDA090747 American Regent, Inc. BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE 3 mg/mL; 3 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0799-01) / 5 mL in 1 VIAL, MULTI-DOSE
76420-007-05 76420-007 HUMAN PRESCRIPTION DRUG Betamethasone Sodium Phosphate and Betamethasone Acetate Betamethasone Sodium Phosphate and Betamethasone Acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR 20200116 N/A ANDA ANDA090747 Asclemed USA, Inc. BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE 3 mg/mL; 3 mg/mL 5 mL in 1 VIAL, MULTI-DOSE (76420-007-05)
0517-0791-01 0517-0791 HUMAN PRESCRIPTION DRUG Betamethasone Sodium Phosphate and Betamethasone Acetate Betamethasone Sodium Phosphate and Betamethasone Acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR 20191101 N/A ANDA ANDA090747 American Regent, Inc. BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE 3 mg/mL; 3 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0791-01) / 5 mL in 1 VIAL, MULTI-DOSE
69263-822-01 69263-822 HUMAN PRESCRIPTION DRUG Beta 1 Kit Betamethasone Sodium Phosphate, Betamethasone Acetate KIT INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR 20150825 N/A ANDA ANDA090747 Oaklock, LLC 1 KIT in 1 CARTON (69263-822-01) * 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0720-01) / 5 mL in 1 VIAL, MULTI-DOSE
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase