NDC 0062-0187 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0062-0187 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021108 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2011-11-02 |
| Marketing End Date | 2015-10-31 |
| Marketing Category | NDA |
| Application Number | NDA021108 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2011-11-02 |
| Marketing End Date | 2015-10-31 |
| Marketing Category | NDA |
| Application Number | NDA021108 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2011-10-18 |
| Marketing End Date | 2015-10-31 |
| Marketing Category | NDA |
| Application Number | NDA021108 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-10-18 |
| Marketing End Date | 2015-10-31 |