| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70954-688-10 | 70954-688 | HUMAN PRESCRIPTION DRUG | Prochlorperazine Maleate | Prochlorperazine Maleate | TABLET | ORAL | 20220801 | N/A | ANDA | ANDA216202 | Novitium Pharma LLC | PROCHLORPERAZINE MALEATE | 5 mg/1 | 100 TABLET in 1 BOTTLE (70954-688-10) |
| 72603-169-01 | 72603-169 | HUMAN PRESCRIPTION DRUG | Prochlorperazine Maleate | Prochlorperazine Maleate | TABLET | ORAL | 20230907 | N/A | ANDA | ANDA216202 | Northstar Rx LLC | PROCHLORPERAZINE MALEATE | 10 mg/1 | 100 TABLET in 1 BOTTLE (72603-169-01) |
| 72603-168-01 | 72603-168 | HUMAN PRESCRIPTION DRUG | Prochlorperazine Maleate | Prochlorperazine Maleate | TABLET | ORAL | 20230907 | N/A | ANDA | ANDA216202 | Northstar Rx LLC | PROCHLORPERAZINE MALEATE | 5 mg/1 | 100 TABLET in 1 BOTTLE (72603-168-01) |
| 70954-689-10 | 70954-689 | HUMAN PRESCRIPTION DRUG | Prochlorperazine Maleate | Prochlorperazine Maleate | TABLET | ORAL | 20220801 | N/A | ANDA | ANDA216202 | Novitium Pharma LLC | PROCHLORPERAZINE MALEATE | 10 mg/1 | 100 TABLET in 1 BOTTLE (70954-689-10) |