NDC 0603-6469 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-6469 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2014-07-24 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2014-07-24 |
| Marketing Category | ANDA |
| Application Number | ANDA078616 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-11-21 |
| Marketing End Date | 2016-12-31 |