| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70518-4195-0 | 70518-4195 | HUMAN PRESCRIPTION DRUG | Anastrozole | Anastrozole | TABLET, FILM COATED | ORAL | 20241001 | N/A | ANDA | ANDA212434 | REMEDYREPACK INC. | ANASTROZOLE | 1 mg/1 | 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4195-0) |
| 59651-236-30 | 59651-236 | HUMAN PRESCRIPTION DRUG | Anastrozole | Anastrozole | TABLET, FILM COATED | ORAL | 20200724 | N/A | ANDA | ANDA212434 | Aurobindo Pharma Limited | ANASTROZOLE | 1 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-236-30) |
| 59651-236-90 | 59651-236 | HUMAN PRESCRIPTION DRUG | Anastrozole | Anastrozole | TABLET, FILM COATED | ORAL | 20200724 | N/A | ANDA | ANDA212434 | Aurobindo Pharma Limited | ANASTROZOLE | 1 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (59651-236-90) |