| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72603-188-01 | 72603-188 | HUMAN PRESCRIPTION DRUG | Dexamethasone | Dexamethasone | TABLET | ORAL | 20230807 | N/A | ANDA | ANDA217696 | NorthStar Rx LLC | DEXAMETHASONE | 2 mg/1 | 100 TABLET in 1 BOTTLE (72603-188-01) |
| 60687-773-01 | 60687-773 | HUMAN PRESCRIPTION DRUG | Dexamethasone | Dexamethasone | TABLET | ORAL | 20231201 | N/A | ANDA | ANDA217696 | American Health Packaging | DEXAMETHASONE | 2 mg/1 | 100 BLISTER PACK in 1 CARTON (60687-773-01) / 1 TABLET in 1 BLISTER PACK (60687-773-11) |
| 72189-523-08 | 72189-523 | HUMAN PRESCRIPTION DRUG | Dexamethasone | Dexamethasone | TABLET | ORAL | 20231113 | N/A | ANDA | ANDA217696 | Direct_Rx | DEXAMETHASONE | 2 mg/1 | 8 TABLET in 1 BOTTLE (72189-523-08) |
| 70954-402-10 | 70954-402 | HUMAN PRESCRIPTION DRUG | Dexamethasone | Dexamethasone | TABLET | ORAL | 20230509 | N/A | ANDA | ANDA217696 | ANI Pharmaceuticals, Inc. | DEXAMETHASONE | 2 mg/1 | 100 TABLET in 1 BOTTLE (70954-402-10) |