NDC 99207-462 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 99207-462 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA050808 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-05-08 |
| Marketing End Date | 2014-02-28 |
| Marketing Category | NDA |
| Application Number | NDA050808 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2006-05-08 |
| Marketing End Date | 2014-02-28 |
| Marketing Category | NDA |
| Application Number | NDA050808 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2006-05-08 |
| Marketing End Date | 2014-02-28 |
| Marketing Category | NDA |
| Application Number | NDA050808 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-05-08 |
| Marketing End Date | 2009-07-28 |