| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0254-2045-02 | 0254-2045 | HUMAN PRESCRIPTION DRUG | POSACONAZOLE | posaconazole | TABLET, COATED | ORAL | 20190830 | N/A | NDA AUTHORIZED GENERIC | NDA205053 | Par Pharmaceutical Inc. | POSACONAZOLE | 100 mg/1 | 60 TABLET, COATED in 1 BOTTLE (0254-2045-02) |
| 63629-2236-1 | 63629-2236 | HUMAN PRESCRIPTION DRUG | POSACONAZOLE | posaconazole | TABLET, COATED | ORAL | 20220901 | N/A | NDA AUTHORIZED GENERIC | NDA205053 | Bryant Ranch Prepack | POSACONAZOLE | 100 mg/1 | 60 TABLET, COATED in 1 BOTTLE (63629-2236-1) |
| 0085-4324-02 | 0085-4324 | HUMAN PRESCRIPTION DRUG | NOXAFIL | posaconazole | TABLET, COATED | ORAL | 20131125 | N/A | NDA | NDA205053 | Merck Sharp & Dohme LLC | POSACONAZOLE | 100 mg/1 | 60 TABLET, COATED in 1 BOTTLE (0085-4324-02) |