NDC 62756-551 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 62756-551 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA091038 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-04-23 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091038 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-04-23 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091038 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-04-23 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091038 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-04-23 |
| Marketing End Date | 2018-04-30 |