NDC 43353-252 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 43353-252 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA202096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-08-03 |
| Marketing End Date | 2012-08-03 |
| Marketing Category | ANDA |
| Application Number | ANDA202096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-08-03 |
| Marketing End Date | 2012-08-03 |