NDC 51079-906 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51079-906 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-11-01 |
| Marketing End Date | 2017-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-06-22 |
| Marketing End Date | 2017-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-08-20 |
| Marketing End Date | 2017-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-11-01 |
| Marketing End Date | 2017-03-31 |