NDC 0378-8127 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0378-8127 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078626 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-05-18 |
| Marketing End Date | 2018-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078626 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-05-18 |
| Marketing End Date | 2015-01-26 |
| Marketing Category | ANDA |
| Application Number | ANDA078626 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-05-29 |
| Marketing End Date | 2018-10-31 |