| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63629-2484-1 | 63629-2484 | HUMAN PRESCRIPTION DRUG | EC-NAPROXEN | naproxen | TABLET, DELAYED RELEASE | ORAL | 20220907 | N/A | NDA | NDA020067 | Bryant Ranch Prepack | NAPROXEN | 500 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63629-2484-1) |
| 90096-161-01 | 90096-161 | HUMAN PRESCRIPTION DRUG | Naproxen | Naproxen | TABLET, DELAYED RELEASE | ORAL | 20250831 | N/A | NDA AUTHORIZED GENERIC | NDA020067 | Zameer Pharmaceuticals LLC | NAPROXEN | 500 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (90096-161-01) |
| 72162-1935-1 | 72162-1935 | HUMAN PRESCRIPTION DRUG | EC-NAPROXEN | naproxen | TABLET, DELAYED RELEASE | ORAL | 20240530 | N/A | NDA | NDA020067 | Bryant Ranch Prepack | NAPROXEN | 500 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1935-1) |