NDC 0069-4170 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0069-4170 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA050797 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1995-06-10 |
| Marketing End Date | 2018-05-31 |
| Marketing Category | NDA |
| Application Number | NDA050797 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1995-06-10 |
| Marketing End Date | 2014-04-07 |
| Marketing Category | NDA |
| Application Number | NDA050797 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1995-06-10 |
| Marketing End Date | 2014-04-07 |