NDC 45802-498 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 45802-498 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078912 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-03-18 |
| Marketing End Date | 2017-02-13 |
| Marketing Category | ANDA |
| Application Number | ANDA078912 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-03-18 |
| Marketing End Date | 2017-01-03 |
| Marketing Category | ANDA |
| Application Number | ANDA078912 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-03-28 |
| Marketing End Date | 2017-02-14 |