NDC 69512-102 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69512-102 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078428 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-10-01 |
| Inactivation Date | 2020-01-31 |