| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0228-3315-03 | 0228-3315 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20200102 | N/A | ANDA | ANDA201951 | Actavis Pharma, Inc. | DOXEPIN HYDROCHLORIDE | 3 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (0228-3315-03) |
| 0228-3316-03 | 0228-3316 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20200102 | N/A | ANDA | ANDA201951 | Actavis Pharma, Inc. | DOXEPIN HYDROCHLORIDE | 6 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (0228-3316-03) |
| 70518-3495-0 | 70518-3495 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20220823 | N/A | ANDA | ANDA201951 | REMEDYREPACK INC. | DOXEPIN HYDROCHLORIDE | 6 mg/1 | 30 POUCH in 1 BOX (70518-3495-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3495-1) |