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=ANDA209253"
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
0480-3315-65 0480-3315 HUMAN PRESCRIPTION DRUG Amphetamine Amphetamine TABLET, ORALLY DISINTEGRATING ORAL 20251208 N/A ANDA ANDA209253 Teva Pharmaceuticals, Inc. AMPHETAMINE 3.1 mg/1 30 BLISTER PACK in 1 CARTON (0480-3315-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
0480-3316-65 0480-3316 HUMAN PRESCRIPTION DRUG Amphetamine Amphetamine TABLET, ORALLY DISINTEGRATING ORAL 20251208 N/A ANDA ANDA209253 Teva Pharmaceuticals, Inc. AMPHETAMINE 6.3 mg/1 30 BLISTER PACK in 1 CARTON (0480-3316-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
0480-3317-65 0480-3317 HUMAN PRESCRIPTION DRUG Amphetamine Amphetamine TABLET, ORALLY DISINTEGRATING ORAL 20251208 N/A ANDA ANDA209253 Teva Pharmaceuticals, Inc. AMPHETAMINE 9.4 mg/1 30 BLISTER PACK in 1 CARTON (0480-3317-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
0480-3318-65 0480-3318 HUMAN PRESCRIPTION DRUG Amphetamine Amphetamine TABLET, ORALLY DISINTEGRATING ORAL 20251208 N/A ANDA ANDA209253 Teva Pharmaceuticals, Inc. AMPHETAMINE 12.5 mg/1 30 BLISTER PACK in 1 CARTON (0480-3318-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
0480-3319-65 0480-3319 HUMAN PRESCRIPTION DRUG Amphetamine Amphetamine TABLET, ORALLY DISINTEGRATING ORAL 20251208 N/A ANDA ANDA209253 Teva Pharmaceuticals, Inc. AMPHETAMINE 15.7 mg/1 30 BLISTER PACK in 1 CARTON (0480-3319-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
0480-3320-65 0480-3320 HUMAN PRESCRIPTION DRUG Amphetamine Amphetamine TABLET, ORALLY DISINTEGRATING ORAL 20251208 N/A ANDA ANDA209253 Teva Pharmaceuticals, Inc. AMPHETAMINE 18.8 mg/1 30 BLISTER PACK in 1 CARTON (0480-3320-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
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