NDC 42507-612 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42507-612 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-08-18 |
| Marketing End Date | 2019-01-24 |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-05-23 |
| Marketing End Date | 2019-03-04 |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-06-12 |
| Marketing End Date | 2019-01-04 |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-05-03 |
| Marketing End Date | 2019-02-24 |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-04-14 |
| Marketing End Date | 2016-10-14 |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-05-23 |
| Marketing End Date | 2015-08-05 |