| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 53401-008-31 | 53401-008 | HUMAN PRESCRIPTION DRUG | Naltrexone Hydrochloride | Naltrexone Hydrochloride | TABLET, FILM COATED | ORAL | 20260414 | 20280630 | ANDA | ANDA075274 | Aphena Pharma Solutions - Tennessee, LLC | NALTREXONE HYDROCHLORIDE | 50 mg/1 | 600 TABLET, FILM COATED in 1 BOTTLE (53401-008-31) |
| 71335-3012-1 | 71335-3012 | HUMAN PRESCRIPTION DRUG | Naltrexone Hydrochloride | Naltrexone Hydrochloride | TABLET, FILM COATED | ORAL | 20251118 | N/A | ANDA | ANDA075274 | Bryant Ranch Prepack | NALTREXONE HYDROCHLORIDE | 50 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-3012-1) |
| 71335-2480-1 | 71335-2480 | HUMAN PRESCRIPTION DRUG | Naltrexone Hydrochloride | Naltrexone Hydrochloride | TABLET, FILM COATED | ORAL | 20240827 | N/A | ANDA | ANDA075274 | Bryant Ranch Prepack | NALTREXONE HYDROCHLORIDE | 50 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2480-1) |