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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0904-7112-70 | 0904-7112 | HUMAN PRESCRIPTION DRUG | Haloperidol | Haloperidol | SOLUTION | ORAL | 19930928 | N/A | ANDA | ANDA073364 | Major Pharmaceuticals | HALOPERIDOL LACTATE | 2 mg/mL | 100 CUP, UNIT-DOSE in 1 CASE (0904-7112-70) / 5 mL in 1 CUP, UNIT-DOSE (0904-7112-41) |
54838-501-15 | 54838-501 | HUMAN PRESCRIPTION DRUG | Haloperidol | Haloperidol | SOLUTION | ORAL | 19930928 | N/A | ANDA | ANDA073364 | Lannett Company, Inc. | HALOPERIDOL LACTATE | 2 mg/mL | 15 mL in 1 BOTTLE, DROPPER (54838-501-15) |
54838-501-40 | 54838-501 | HUMAN PRESCRIPTION DRUG | Haloperidol | Haloperidol | SOLUTION | ORAL | 19930928 | N/A | ANDA | ANDA073364 | Lannett Company, Inc. | HALOPERIDOL LACTATE | 2 mg/mL | 120 mL in 1 BOTTLE, DROPPER (54838-501-40) |