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=ANDA208606"
符合检索条件的记录共 12 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
72241-020-05 72241-020 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Modavar Pharmaceuticals LLC BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72241-020-05)
72241-020-11 72241-020 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Modavar Pharmaceuticals LLC BUPROPION HYDROCHLORIDE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72241-020-11)
72241-020-17 72241-020 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Modavar Pharmaceuticals LLC BUPROPION HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 CARTON (72241-020-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK
72241-021-05 72241-021 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Modavar Pharmaceuticals LLC BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72241-021-05)
72241-021-11 72241-021 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Modavar Pharmaceuticals LLC BUPROPION HYDROCHLORIDE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72241-021-11)
72241-021-17 72241-021 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Modavar Pharmaceuticals LLC BUPROPION HYDROCHLORIDE 100 mg/1 10 BLISTER PACK in 1 CARTON (72241-021-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK
71209-052-05 71209-052 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Cadila Pharmaceuticals Limited BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71209-052-05)
71209-052-11 71209-052 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Cadila Pharmaceuticals Limited BUPROPION HYDROCHLORIDE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (71209-052-11)
71209-052-17 71209-052 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Cadila Pharmaceuticals Limited BUPROPION HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 CARTON (71209-052-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK
71209-053-05 71209-053 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Cadila Pharmaceuticals Limited BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71209-053-05)
71209-053-11 71209-053 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Cadila Pharmaceuticals Limited BUPROPION HYDROCHLORIDE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (71209-053-11)
71209-053-17 71209-053 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230112 N/A ANDA ANDA208606 Cadila Pharmaceuticals Limited BUPROPION HYDROCHLORIDE 100 mg/1 10 BLISTER PACK in 1 CARTON (71209-053-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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