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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
ULTRAVATE | 019968 | 001 | NDA | HALOBETASOL PROPIONATE | OINTMENT;TOPICAL | 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 1990/12/17 | 1990/12/17 | SUN PHARM INDS INC | Discontinued |
ULTRAVATE | 019967 | 001 | NDA | HALOBETASOL PROPIONATE | CREAM;TOPICAL | 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Yes | No | 1990/12/27 | 1990/12/27 | SUN PHARM INDS INC | Discontinued |
ULTRAVATE | 208183 | 001 | NDA | HALOBETASOL PROPIONATE | LOTION;TOPICAL | 0.05% | Yes | Yes | 2015/11/06 | 2015/11/06 | SUN PHARM INDUSTRIES | Prescription |