| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 68084-083-01 | 68084-083 | HUMAN PRESCRIPTION DRUG | Isosorbide Dinitrate | Isosorbide Dinitrate | TABLET | ORAL | 20131021 | N/A | ANDA | ANDA087537 | American Health Packaging | ISOSORBIDE DINITRATE | 20 mg/1 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-083-01) / 1 TABLET in 1 BLISTER PACK (68084-083-11) |
| 50268-449-15 | 50268-449 | HUMAN PRESCRIPTION DRUG | Isosorbide Dinitrate | isosorbide dinitrate | TABLET | ORAL | 20160913 | N/A | ANDA | ANDA087537 | AvPAK | ISOSORBIDE DINITRATE | 20 mg/1 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-449-15) / 1 TABLET in 1 BLISTER PACK (50268-449-11) |
| 49884-022-01 | 49884-022 | HUMAN PRESCRIPTION DRUG | Isosorbide Dinitrate | isosorbide dinitrate | TABLET | ORAL | 19811215 | N/A | ANDA | ANDA087537 | Endo USA, Inc. | ISOSORBIDE DINITRATE | 20 mg/1 | 100 TABLET in 1 BOTTLE (49884-022-01) |
| 49884-022-10 | 49884-022 | HUMAN PRESCRIPTION DRUG | Isosorbide Dinitrate | isosorbide dinitrate | TABLET | ORAL | 19811215 | N/A | ANDA | ANDA087537 | Endo USA, Inc. | ISOSORBIDE DINITRATE | 20 mg/1 | 1000 TABLET in 1 BOTTLE (49884-022-10) |