NDC 62037-720 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 62037-720 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075604 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-04-10 |
| Marketing End Date | 2017-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075604 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-04-10 |
| Marketing End Date | 2015-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075604 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-04-10 |
| Marketing End Date | 2017-08-31 |