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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
59011-415-20 | 59011-415 | HUMAN PRESCRIPTION DRUG | OxyContin | oxycodone hydrochloride | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20100808 | N/A | NDA | NDA022272 | Purdue Pharma LP | OXYCODONE HYDROCHLORIDE | 15 mg/1 | 2 BLISTER PACK in 1 CARTON (59011-415-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
59011-410-10 | 59011-410 | HUMAN PRESCRIPTION DRUG | OxyContin | oxycodone hydrochloride | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20100808 | N/A | NDA | NDA022272 | Purdue Pharma LP | OXYCODONE HYDROCHLORIDE | 10 mg/1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-410-10) |