| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72819-162-03 | 72819-162 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20220221 | N/A | ANDA | ANDA202337 | Archis Pharma LLC | DOXEPIN HYDROCHLORIDE | 6 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72819-162-03) |
| 72819-162-10 | 72819-162 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20220221 | N/A | ANDA | ANDA202337 | Archis Pharma LLC | DOXEPIN HYDROCHLORIDE | 6 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (72819-162-10) |
| 72819-162-11 | 72819-162 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20220221 | N/A | ANDA | ANDA202337 | Archis Pharma LLC | DOXEPIN HYDROCHLORIDE | 6 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (72819-162-11) |
| 72819-161-11 | 72819-161 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20220221 | N/A | ANDA | ANDA202337 | Archis Pharma LLC | DOXEPIN HYDROCHLORIDE | 3 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (72819-161-11) |
| 72819-161-10 | 72819-161 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20220221 | N/A | ANDA | ANDA202337 | Archis Pharma LLC | DOXEPIN HYDROCHLORIDE | 3 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (72819-161-10) |
| 72819-161-03 | 72819-161 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20220221 | N/A | ANDA | ANDA202337 | Archis Pharma LLC | DOXEPIN HYDROCHLORIDE | 3 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72819-161-03) |
| 10135-758-30 | 10135-758 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20231001 | N/A | ANDA | ANDA202337 | Marlex Pharmaceuticals, Inc. | DOXEPIN HYDROCHLORIDE | 3 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (10135-758-30) |
| 10135-764-30 | 10135-764 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20231001 | N/A | ANDA | ANDA202337 | Marlex Pharmaceuticals, Inc. | DOXEPIN HYDROCHLORIDE | 6 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (10135-764-30) |
| 72603-223-01 | 72603-223 | HUMAN PRESCRIPTION DRUG | Doxepin | Doxepin | TABLET, FILM COATED | ORAL | 20240401 | N/A | ANDA | ANDA202337 | North Star Rx LLC | DOXEPIN HYDROCHLORIDE | 6 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72603-223-01) |
符合检索条件的记录共 9 条，共 1 页，当前第 1 页 ，
可点击列名称排序
可点击列名称排序