NDC 0172-2908 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-2908 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018413 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1983-11-30 |
| Marketing End Date | 2018-03-31 |
| Marketing Category | NDA |
| Application Number | NDA018413 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-07-26 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | NDA |
| Application Number | NDA018413 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1983-11-30 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | NDA |
| Application Number | NDA018413 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1983-11-30 |
| Marketing End Date | 2012-02-29 |