| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0456-2005-01 | 0456-2005 | HUMAN PRESCRIPTION DRUG | Lexapro | ESCITALOPRAM | TABLET, FILM COATED | ORAL | 20020814 | N/A | NDA | NDA021323 | Allergan, Inc. | ESCITALOPRAM OXALATE | 5 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0456-2005-01) |
| 0456-2010-01 | 0456-2010 | HUMAN PRESCRIPTION DRUG | Lexapro | ESCITALOPRAM | TABLET, FILM COATED | ORAL | 20020814 | N/A | NDA | NDA021323 | Allergan, Inc. | ESCITALOPRAM OXALATE | 10 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0456-2010-01) |
| 0456-2020-01 | 0456-2020 | HUMAN PRESCRIPTION DRUG | Lexapro | ESCITALOPRAM | TABLET, FILM COATED | ORAL | 20020814 | N/A | NDA | NDA021323 | Allergan, Inc. | ESCITALOPRAM OXALATE | 20 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0456-2020-01) |