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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
42806-005-01 | 42806-005 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydrochloride | Oxycodone Hydrochloride | TABLET | ORAL | 20150922 | N/A | ANDA | ANDA202662 | Epic Pharma, LLC | OXYCODONE HYDROCHLORIDE | 5 mg/1 | 100 TABLET in 1 BOTTLE (42806-005-01) |
42806-006-01 | 42806-006 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydrochloride | Oxycodone Hydrochloride | TABLET | ORAL | 20150922 | N/A | ANDA | ANDA202662 | Epic Pharma, LLC | OXYCODONE HYDROCHLORIDE | 10 mg/1 | 100 TABLET in 1 BOTTLE (42806-006-01) |
42806-007-01 | 42806-007 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydrochloride | Oxycodone Hydrochloride | TABLET | ORAL | 20150922 | N/A | ANDA | ANDA202662 | Epic Pharma, LLC | OXYCODONE HYDROCHLORIDE | 15 mg/1 | 100 TABLET in 1 BOTTLE (42806-007-01) |
42806-008-01 | 42806-008 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydrochloride | Oxycodone Hydrochloride | TABLET | ORAL | 20150922 | N/A | ANDA | ANDA202662 | Epic Pharma, LLC | OXYCODONE HYDROCHLORIDE | 30 mg/1 | 100 TABLET in 1 BOTTLE (42806-008-01) |
42806-009-01 | 42806-009 | HUMAN PRESCRIPTION DRUG | Oxycodone Hydrochloride | Oxycodone Hydrochloride | TABLET | ORAL | 20170516 | N/A | ANDA | ANDA202662 | Epic Pharma, LLC | OXYCODONE HYDROCHLORIDE | 20 mg/1 | 100 TABLET in 1 BOTTLE (42806-009-01) |