NDC 0781-1223 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-1223 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073288 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-03-25 |
| Marketing End Date | 2013-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073288 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-03-25 |
| Marketing End Date | 2013-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073288 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-03-25 |
| Marketing End Date | 2013-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073288 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-03-25 |
| Marketing End Date | 2013-08-31 |