NDC 64720-138 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 64720-138 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076347 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-06 |
| Marketing End Date | 2012-10-01 |
| Marketing Category | ANDA |
| Application Number | ANDA076347 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-06 |
| Marketing End Date | 2012-10-01 |
| Marketing Category | ANDA |
| Application Number | ANDA076347 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-06 |
| Marketing End Date | 2012-10-01 |