NDC 0093-5171 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-5171 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075710 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-06-14 |
| Marketing End Date | 2018-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075710 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-02-06 |
| Marketing End Date | 2014-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075710 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-02-06 |
| Marketing End Date | 2018-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075710 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-02-06 |
| Marketing End Date | 2018-05-31 |