NDC 0074-6316 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0074-6316 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA060359 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1964-06-24 |
| Marketing End Date | 2015-06-29 |