| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 75907-022-01 | 75907-022 | HUMAN PRESCRIPTION DRUG | Carbidopa and Levodopa | Carbidopa and Levodopa | TABLET | ORAL | 20240501 | N/A | ANDA | ANDA073618 | Dr. Reddy's Laboratories Inc | CARBIDOPA; LEVODOPA | 10 mg/1; 100 mg/1 | 100 TABLET in 1 BOTTLE (75907-022-01) |
| 51862-855-01 | 51862-855 | HUMAN PRESCRIPTION DRUG | Carbidopa and Levodopa | Carbidopa and Levodopa | TABLET | ORAL | 20180716 | N/A | ANDA | ANDA073618 | Mayne Pharma Commercial LLC | CARBIDOPA; LEVODOPA | 10 mg/1; 100 mg/1 | 100 TABLET in 1 BOTTLE (51862-855-01) |
| 51862-855-05 | 51862-855 | HUMAN PRESCRIPTION DRUG | Carbidopa and Levodopa | Carbidopa and Levodopa | TABLET | ORAL | 20180716 | N/A | ANDA | ANDA073618 | Mayne Pharma Commercial LLC | CARBIDOPA; LEVODOPA | 10 mg/1; 100 mg/1 | 500 TABLET in 1 BOTTLE (51862-855-05) |