| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-0723-8 | 71335-0723 | HUMAN PRESCRIPTION DRUG | HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | TABLET | ORAL | 20240809 | N/A | ANDA | ANDA205814 | Bryant Ranch Prepack | HYDROMORPHONE HYDROCHLORIDE | 4 mg/1 | 56 TABLET in 1 BOTTLE (71335-0723-8) |
| 71335-0723-9 | 71335-0723 | HUMAN PRESCRIPTION DRUG | HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | TABLET | ORAL | 20240809 | N/A | ANDA | ANDA205814 | Bryant Ranch Prepack | HYDROMORPHONE HYDROCHLORIDE | 4 mg/1 | 140 TABLET in 1 BOTTLE (71335-0723-9) |