NDC 0093-8122 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-8122 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075536 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-12-08 |
| Marketing End Date | 2013-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075536 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-10-20 |
| Marketing End Date | 2015-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075536 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-10 |
| Marketing End Date | 2015-08-31 |