NDC 43063-358 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 43063-358 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA019885 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-01-30 |
| Marketing End Date | 2016-08-31 |
| Marketing Category | NDA authorized generic |
| Application Number | NDA019885 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-01-30 |
| Marketing End Date | 2016-08-31 |