NDC 63402-513 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63402-513 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020837 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-12-21 |
| Marketing End Date | 2014-04-08 |
| Marketing Category | NDA |
| Application Number | NDA020837 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-12-21 |
| Marketing End Date | 2014-04-08 |
| Marketing Category | NDA |
| Application Number | NDA020837 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1999-04-01 |
| Marketing End Date | 2017-02-28 |
| Marketing Category | NDA |
| Application Number | NDA020837 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-12-21 |
| Marketing End Date | 2014-04-08 |
| Marketing Category | NDA |
| Application Number | NDA020837 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1999-04-01 |
| Marketing End Date | 2017-02-28 |