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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
42571-275-60 | 42571-275 | HUMAN PRESCRIPTION DRUG | DALFAMPRIDINE | DALFAMPRIDINE | TABLET, EXTENDED RELEASE | ORAL | 20190321 | N/A | ANDA | ANDA210158 | Micro Labs Limited | DALFAMPRIDINE | 10 mg/1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-275-60) |
42571-275-10 | 42571-275 | HUMAN PRESCRIPTION DRUG | DALFAMPRIDINE | DALFAMPRIDINE | TABLET, EXTENDED RELEASE | ORAL | 20190321 | N/A | ANDA | ANDA210158 | Micro Labs Limited | DALFAMPRIDINE | 10 mg/1 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-275-10) |
42571-275-05 | 42571-275 | HUMAN PRESCRIPTION DRUG | DALFAMPRIDINE | DALFAMPRIDINE | TABLET, EXTENDED RELEASE | ORAL | 20190321 | N/A | ANDA | ANDA210158 | Micro Labs Limited | DALFAMPRIDINE | 10 mg/1 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-275-05) |