| 商品名 | 申请号 | 产品号 | 申请类型 | 活性成分 | 剂型/给药途径 | 规格/剂量 | RLD | RS | 申请号原始批准/暂定批准日期 | 产品号批准日期 | 申请人 | 市场状态 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| SODIUM CHLORIDE IN PLASTIC CONTAINER | 018247 | 001 | NDA | SODIUM CHLORIDE | SOLUTION;IRRIGATION | 900MG/100ML | No | No | -- | Approved Prior to Jan 1, 1982 | MILES | Discontinued |
| CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER | 062422 | 001 | ANDA | CEPHALOTHIN SODIUM | INJECTABLE;INJECTION | EQ 20MG BASE/ML | No | No | 1984/01/31 | 1984/01/31 | BAXTER HLTHCARE | Discontinued |
| CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER | 062422 | 002 | ANDA | CEPHALOTHIN SODIUM | INJECTABLE;INJECTION | EQ 40MG BASE/ML | No | No | 1984/01/31 | 1984/01/31 | BAXTER HLTHCARE | Discontinued |
| CARDENE IN 0.86% SODIUM CHLORIDE IN PLASTIC CONTAINER | 019734 | 003 | NDA | NICARDIPINE HYDROCHLORIDE | INJECTABLE;INTRAVENOUS | 20MG/200ML (0.1MG/ML) | Yes | Yes | 1992/01/30 | 2008/07/31 | CHIESI | Prescription |
| CARDENE IN 0.83% SODIUM CHLORIDE IN PLASTIC CONTAINER | 019734 | 004 | NDA | NICARDIPINE HYDROCHLORIDE | INJECTABLE;INTRAVENOUS | 40MG/200ML (0.2MG/ML) | Yes | Yes | 1992/01/30 | 2008/11/07 | CHIESI | Prescription |