NDC 0135-0132 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0135-0132 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-03-29 |
| Marketing End Date | 2018-09-30 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-03-29 |
| Marketing End Date | 2018-09-30 |