| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 13668-760-60 | 13668-760 | HUMAN PRESCRIPTION DRUG | Ranolazine | Ranolazine | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20260511 | N/A | ANDA | ANDA214035 | Torrent Pharma, Inc. | RANOLAZINE | 1000 mg/1 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (13668-760-60) |
| 13668-759-60 | 13668-759 | HUMAN PRESCRIPTION DRUG | Ranolazine | Ranolazine | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20260511 | N/A | ANDA | ANDA214035 | Torrent Pharma, Inc. | RANOLAZINE | 500 mg/1 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (13668-759-60) |