NDC 0904-6344 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0904-6344 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-02-03 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-02-03 |
| Marketing End Date | 2016-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-02-03 |
| Marketing End Date | 2017-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-02-03 |
| Marketing End Date | 2015-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-02-03 |
| Marketing End Date | 2015-12-31 |