| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0781-8017-31 | 0781-8017 | HUMAN PRESCRIPTION DRUG | FLUVASTATIN SODIUM ER | fluvastatin sodium | TABLET, EXTENDED RELEASE | ORAL | 20180502 | N/A | NDA AUTHORIZED GENERIC | NDA021192 | Sandoz Inc | FLUVASTATIN SODIUM | 80 mg/1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-31) |
| 0781-8017-01 | 0781-8017 | HUMAN PRESCRIPTION DRUG | FLUVASTATIN SODIUM ER | fluvastatin sodium | TABLET, EXTENDED RELEASE | ORAL | 20180502 | N/A | NDA AUTHORIZED GENERIC | NDA021192 | Sandoz Inc | FLUVASTATIN SODIUM | 80 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-01) |
| 0078-0354-15 | 0078-0354 | HUMAN PRESCRIPTION DRUG | Lescol XL | fluvastatin sodium | TABLET, EXTENDED RELEASE | ORAL | 20001006 | N/A | NDA | NDA021192 | Novartis Pharmaceuticals Corporation | FLUVASTATIN SODIUM | 80 mg/1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0078-0354-15) |