NDC 59762-0245 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59762-0245 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020690 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-11-26 |
| Marketing End Date | 2017-07-31 |
| Marketing Category | NDA |
| Application Number | NDA020690 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-11-26 |
| Marketing End Date | 2017-07-31 |
| Marketing Category | NDA |
| Application Number | NDA020690 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-11-26 |
| Marketing End Date | 2017-07-31 |
| Marketing Category | NDA |
| Application Number | NDA020690 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-11-26 |
| Marketing End Date | 2017-07-31 |