NDC 0472-5242 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0472-5242 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075014 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2000-06-11 |
| Marketing End Date | 2017-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075014 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2000-06-11 |
| Marketing End Date | 2017-04-30 |