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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
23155-628-01 | 23155-628 | HUMAN PRESCRIPTION DRUG | Isosorbide Mononitrate | Isosorbide Mononitrate | TABLET, EXTENDED RELEASE | ORAL | 20181115 | N/A | ANDA | ANDA210822 | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ISOSORBIDE MONONITRATE | 120 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-628-01) |
42799-960-01 | 42799-960 | HUMAN PRESCRIPTION DRUG | Isosorbide Mononitrate | Isosorbide Mononitrate | TABLET, EXTENDED RELEASE | ORAL | 20230701 | N/A | ANDA | ANDA210822 | Edenbridge Pharmaceuticals LLC. | ISOSORBIDE MONONITRATE | 120 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42799-960-01) |
62135-588-90 | 62135-588 | HUMAN PRESCRIPTION DRUG | Isosorbide Mononitrate | Isosorbide Mononitrate | TABLET, EXTENDED RELEASE | ORAL | 20230426 | N/A | ANDA | ANDA210822 | Chartwell RX, LLC | ISOSORBIDE MONONITRATE | 120 mg/1 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-588-90) |