NDC 60505-0025 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60505-0025 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074680 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-09-13 |
| Marketing End Date | 2012-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074680 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-09-13 |
| Marketing End Date | 2012-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074680 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-09-13 |
| Marketing End Date | 2012-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074680 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-09-13 |
| Marketing End Date | 2012-12-31 |