NDC 0074-3079 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0074-3079 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020381 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-07-28 |
| Marketing End Date | 2009-06-29 |
| Marketing Category | NDA |
| Application Number | NDA020381 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-07-28 |
| Marketing End Date | 2018-12-01 |
| Marketing Category | NDA |
| Application Number | NDA020381 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-07-28 |
| Marketing End Date | 2011-02-13 |