| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0093-7536-56 | 0093-7536 | HUMAN PRESCRIPTION DRUG | Anastrozole | Anastrozole | TABLET, FILM COATED | ORAL | 20100628 | N/A | ANDA | ANDA078058 | Teva Pharmaceuticals USA, Inc. | ANASTROZOLE | 1 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56) |
| 42291-085-30 | 42291-085 | HUMAN PRESCRIPTION DRUG | Anastrozole | Anastrozole | TABLET, FILM COATED | ORAL | 20200313 | N/A | ANDA | ANDA078058 | AvKARE | ANASTROZOLE | 1 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-085-30) |
| 42291-085-90 | 42291-085 | HUMAN PRESCRIPTION DRUG | Anastrozole | Anastrozole | TABLET, FILM COATED | ORAL | 20200923 | N/A | ANDA | ANDA078058 | AvKARE | ANASTROZOLE | 1 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (42291-085-90) |