NDC 0173-0344 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0173-0344 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018703 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1989-10-01 |
| Marketing End Date | 2017-05-31 |
| Marketing Category | NDA |
| Application Number | NDA018703 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1989-10-01 |
| Marketing End Date | 2016-06-30 |
| Marketing Category | NDA |
| Application Number | NDA018703 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1989-10-01 |
| Marketing End Date | 2011-10-03 |