| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1099-8 | 71335-1099 | HUMAN PRESCRIPTION DRUG | CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | TABLET, FILM COATED | ORAL | 20190222 | N/A | ANDA | ANDA208170 | Bryant Ranch Prepack | CYCLOBENZAPRINE HYDROCHLORIDE | 5 mg/1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1099-8) |
| 71335-1099-9 | 71335-1099 | HUMAN PRESCRIPTION DRUG | CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | TABLET, FILM COATED | ORAL | 20190222 | N/A | ANDA | ANDA208170 | Bryant Ranch Prepack | CYCLOBENZAPRINE HYDROCHLORIDE | 5 mg/1 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1099-9) |