| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 24658-720-01 | 24658-720 | HUMAN PRESCRIPTION DRUG | Flavoxate Hydrochloride | Flavoxate Hydrochloride | TABLET | ORAL | 20161215 | N/A | ANDA | ANDA076835 | PuraCap Laboratories LLC dba Blu Pharmaceuticals | FLAVOXATE HYDROCHLORIDE | 100 mg/1 | 100 TABLET in 1 BOTTLE (24658-720-01) |
| 42806-058-01 | 42806-058 | HUMAN PRESCRIPTION DRUG | Flavoxate Hydrochloride | Flavoxate Hydrochloride | TABLET | ORAL | 20110221 | N/A | ANDA | ANDA076835 | Epic Pharma, LLC | FLAVOXATE HYDROCHLORIDE | 100 mg/1 | 100 TABLET in 1 BOTTLE (42806-058-01) |
| 42806-058-10 | 42806-058 | HUMAN PRESCRIPTION DRUG | Flavoxate Hydrochloride | Flavoxate Hydrochloride | TABLET | ORAL | 20110221 | N/A | ANDA | ANDA076835 | Epic Pharma, LLC | FLAVOXATE HYDROCHLORIDE | 100 mg/1 | 1000 TABLET in 1 BOTTLE (42806-058-10) |