NDC 37205-280 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 37205-280 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075794 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-05-16 |
| Marketing End Date | 2019-03-26 |
| Marketing Category | ANDA |
| Application Number | ANDA075794 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-05-16 |
| Marketing End Date | 2019-03-26 |