NDC 0472-1262 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0472-1262 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074916 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1999-04-30 |
| Marketing End Date | 1999-04-30 |