NDC 11673-022 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 11673-022 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075285 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-05-12 |
| Marketing End Date | 2015-01-20 |