| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 51655-461-52 | 51655-461 | HUMAN PRESCRIPTION DRUG | Desmopressin Acetate | Desmopressin Acetate | TABLET | ORAL | 20201029 | N/A | ANDA | ANDA210371 | Northwind Pharmaceuticals, LLC | DESMOPRESSIN ACETATE | .2 mg/1 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-461-52) |
| 10702-170-01 | 10702-170 | HUMAN PRESCRIPTION DRUG | Desmopressin Acetate | Desmopressin Acetate | TABLET | ORAL | 20190128 | N/A | ANDA | ANDA210371 | KVK-TECH, INC. | DESMOPRESSIN ACETATE | .2 mg/1 | 100 TABLET in 1 BOTTLE (10702-170-01) |
| 10702-169-01 | 10702-169 | HUMAN PRESCRIPTION DRUG | Desmopressin Acetate | Desmopressin Acetate | TABLET | ORAL | 20190128 | N/A | ANDA | ANDA210371 | KVK-TECH, INC. | DESMOPRESSIN ACETATE | .1 mg/1 | 100 TABLET in 1 BOTTLE (10702-169-01) |