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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0456-4010-01 | 0456-4010 | HUMAN PRESCRIPTION DRUG | Celexa | citalopram | TABLET, FILM COATED | ORAL | 19980717 | N/A | NDA | NDA020822 | Allergan, Inc. | CITALOPRAM HYDROBROMIDE | 10 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0456-4010-01) |
0456-4020-01 | 0456-4020 | HUMAN PRESCRIPTION DRUG | Celexa | citalopram | TABLET, FILM COATED | ORAL | 19980717 | N/A | NDA | NDA020822 | Allergan, Inc. | CITALOPRAM HYDROBROMIDE | 20 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0456-4020-01) |
0456-4040-01 | 0456-4040 | HUMAN PRESCRIPTION DRUG | Celexa | citalopram | TABLET, FILM COATED | ORAL | 19980717 | N/A | NDA | NDA020822 | Allergan, Inc. | CITALOPRAM HYDROBROMIDE | 40 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0456-4040-01) |