NDC 0049-1620 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0049-1620 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020329 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-04-26 |
| Marketing End Date | 2014-01-31 |