| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72162-1347-3 | 72162-1347 | HUMAN PRESCRIPTION DRUG | Buprenorphine and Naloxone | Buprenorphine and Naloxone | TABLET | SUBLINGUAL | 20240312 | N/A | ANDA | ANDA205601 | Bryant Ranch Prepack | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE | 8 mg/1; 2 mg/1 | 30 TABLET in 1 BOTTLE, PLASTIC (72162-1347-3) |
| 70518-3389-0 | 70518-3389 | HUMAN PRESCRIPTION DRUG | Buprenorphine and Naloxone | Buprenorphine and Naloxone | TABLET | SUBLINGUAL | 20220316 | N/A | ANDA | ANDA205601 | REMEDYREPACK INC. | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE | 8 mg/1; 2 mg/1 | 30 TABLET in 1 BLISTER PACK (70518-3389-0) |