NDC 43386-350 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 43386-350 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA091528 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-01-24 |
| Marketing End Date | 2014-09-19 |
| Marketing Category | ANDA |
| Application Number | ANDA091528 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-02-16 |
| Marketing End Date | 2014-09-19 |
| Marketing Category | ANDA |
| Application Number | ANDA091528 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-02-16 |
| Marketing End Date | 2014-09-19 |