| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82293-002-10 | 82293-002 | HUMAN PRESCRIPTION DRUG | Abiraterone Acetate | abiraterone acetate | TABLET, FILM COATED | ORAL | 20220105 | N/A | ANDA | ANDA215947 | Novugen Pharma (USA) LLC | ABIRATERONE ACETATE | 500 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82293-002-10) |
| 82293-001-10 | 82293-001 | HUMAN PRESCRIPTION DRUG | Abiraterone Acetate | abiraterone acetate | TABLET, FILM COATED | ORAL | 20220105 | N/A | ANDA | ANDA215947 | Novugen Pharma (USA) LLC | ABIRATERONE ACETATE | 250 mg/1 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82293-001-10) |