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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
42799-207-01 | 42799-207 | HUMAN PRESCRIPTION DRUG | Tinidazole | Tinidazole | TABLET | ORAL | 20191220 | N/A | ANDA | ANDA203808 | Edenbridge Pharmaceuticals LLC. | TINIDAZOLE | 250 mg/1 | 40 TABLET in 1 BOTTLE (42799-207-01) |
42799-208-01 | 42799-208 | HUMAN PRESCRIPTION DRUG | Tinidazole | Tinidazole | TABLET | ORAL | 20191220 | N/A | ANDA | ANDA203808 | Edenbridge Pharmaceuticals LLC. | TINIDAZOLE | 500 mg/1 | 20 TABLET in 1 BOTTLE (42799-208-01) |
42799-208-02 | 42799-208 | HUMAN PRESCRIPTION DRUG | Tinidazole | Tinidazole | TABLET | ORAL | 20191220 | N/A | ANDA | ANDA203808 | Edenbridge Pharmaceuticals LLC. | TINIDAZOLE | 500 mg/1 | 60 TABLET in 1 BOTTLE (42799-208-02) |