NDC 0062-0175 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0062-0175 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA017522 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1974-07-30 |
| Marketing End Date | 2015-07-31 |
| Marketing Category | NDA |
| Application Number | NDA017522 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1974-07-30 |
| Marketing End Date | 2015-06-30 |