NDC 49884-821 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49884-821 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078783 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-06-28 |
| Marketing End Date | 2018-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078783 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-06-28 |
| Marketing End Date | 2017-06-21 |
| Marketing Category | ANDA |
| Application Number | ANDA078783 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-06-28 |
| Marketing End Date | 2017-01-11 |
| Marketing Category | ANDA |
| Application Number | ANDA078783 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-06-28 |
| Marketing End Date | 2011-01-06 |