NDC 53746-118 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 53746-118 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040769 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-02-18 |
| Marketing End Date | 2014-04-01 |
| Marketing Category | ANDA |
| Application Number | ANDA040769 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-02-18 |
| Marketing End Date | 2014-04-01 |
| Marketing Category | ANDA |
| Application Number | ANDA040769 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-10-14 |
| Marketing End Date | 2014-04-01 |