NDC 0093-0784 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-0784 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075797 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-02-20 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA075797 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-01-09 |
| Marketing End Date | 2017-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075797 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-02-20 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA075797 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-01-09 |
| Marketing End Date | 2018-02-28 |