NDC 49999-847 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49999-847 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076438 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-12-13 |
| Marketing End Date | 2014-06-01 |
| Marketing Category | ANDA |
| Application Number | ANDA076438 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-12-13 |
| Marketing End Date | 2014-06-01 |
| Marketing Category | ANDA |
| Application Number | ANDA076438 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-08-19 |
| Marketing End Date | 2018-12-14 |
| Marketing Category | ANDA |
| Application Number | ANDA076438 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-12-13 |
| Marketing End Date | 2014-06-01 |