| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1245-5 | 71335-1245 | HUMAN PRESCRIPTION DRUG | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | TABLET | ORAL | 20240709 | N/A | ANDA | ANDA091393 | Bryant Ranch Prepack | OXYCODONE HYDROCHLORIDE | 30 mg/1 | 100 TABLET in 1 BOTTLE (71335-1245-5) |
| 71335-1245-6 | 71335-1245 | HUMAN PRESCRIPTION DRUG | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | TABLET | ORAL | 20240709 | N/A | ANDA | ANDA091393 | Bryant Ranch Prepack | OXYCODONE HYDROCHLORIDE | 30 mg/1 | 40 TABLET in 1 BOTTLE (71335-1245-6) |
| 71335-1245-7 | 71335-1245 | HUMAN PRESCRIPTION DRUG | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | TABLET | ORAL | 20240709 | N/A | ANDA | ANDA091393 | Bryant Ranch Prepack | OXYCODONE HYDROCHLORIDE | 30 mg/1 | 18 TABLET in 1 BOTTLE (71335-1245-7) |
| 71335-1245-8 | 71335-1245 | HUMAN PRESCRIPTION DRUG | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | TABLET | ORAL | 20240709 | N/A | ANDA | ANDA091393 | Bryant Ranch Prepack | OXYCODONE HYDROCHLORIDE | 30 mg/1 | 28 TABLET in 1 BOTTLE (71335-1245-8) |
| 72189-611-30 | 72189-611 | HUMAN PRESCRIPTION DRUG | Oxycodone HCL | Oxycodone HCL | TABLET | ORAL | 20250324 | N/A | ANDA | ANDA091393 | Direct_Rx | OXYCODONE HYDROCHLORIDE | 5 mg/1 | 30 TABLET in 1 BOTTLE (72189-611-30) |