NDC 46122-205 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 46122-205 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075400 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-10-07 |
| Marketing End Date | 2019-01-22 |
| Marketing Category | ANDA |
| Application Number | ANDA075400 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-10-07 |
| Marketing End Date | 2019-01-22 |