NDC 24987-242 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 24987-242 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020405 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-09-30 |
| Marketing End Date | 2017-09-30 |
| Marketing Category | NDA |
| Application Number | NDA020405 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-09-30 |
| Marketing End Date | 2018-08-31 |
| Marketing Category | NDA |
| Application Number | NDA020405 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-09-30 |
| Marketing End Date | 2018-08-31 |
| Marketing Category | NDA |
| Application Number | NDA020405 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-09-30 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | NDA |
| Application Number | NDA020405 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-09-30 |
| Marketing End Date | 2018-11-30 |