NDC 0006-0711 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0006-0711 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020830 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-02-20 |
| Marketing End Date | 2015-01-31 |
| Marketing Category | NDA |
| Application Number | NDA020830 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-02-20 |
| Marketing End Date | 2013-09-19 |
| Marketing Category | NDA |
| Application Number | NDA020830 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-02-20 |
| Marketing End Date | 2015-01-31 |
| Marketing Category | NDA |
| Application Number | NDA020830 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-15 |
| Marketing End Date | 2014-06-10 |
| Marketing Category | NDA |
| Application Number | NDA020830 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-02-20 |
| Marketing End Date | 2013-09-19 |