| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 43063-761-90 | 43063-761 | HUMAN PRESCRIPTION DRUG | escitalopram oxalate | escitalopram oxalate | TABLET, FILM COATED | ORAL | 20170503 | N/A | ANDA | ANDA090939 | PD-Rx Pharmaceuticals, Inc. | ESCITALOPRAM OXALATE | 10 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-90) |
| 82982-065-60 | 82982-065 | HUMAN PRESCRIPTION DRUG | escitalopram oxalate | escitalopram oxalate | TABLET | ORAL | 20230501 | 20260731 | ANDA | ANDA090939 | Pharmasource Meds, LLC | ESCITALOPRAM OXALATE | 10 mg/1 | 60 TABLET in 1 BOTTLE (82982-065-60) |
| 72189-438-30 | 72189-438 | HUMAN PRESCRIPTION DRUG | Escitalopram | Escitalopram | TABLET | ORAL | 20230313 | N/A | ANDA | ANDA090939 | Direct_Rx | ESCITALOPRAM OXALATE | 20 mg/1 | 30 TABLET in 1 BOTTLE (72189-438-30) |
| 72189-438-90 | 72189-438 | HUMAN PRESCRIPTION DRUG | Escitalopram | Escitalopram | TABLET | ORAL | 20230313 | N/A | ANDA | ANDA090939 | Direct_Rx | ESCITALOPRAM OXALATE | 20 mg/1 | 90 TABLET in 1 BOTTLE (72189-438-90) |