NDC 0904-5591 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0904-5591 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076494 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-04-01 |
| Marketing End Date | 2015-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076494 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-04-01 |
| Marketing End Date | 2014-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076494 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-04-01 |
| Marketing End Date | 2015-09-30 |