NDC 0093-4740 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-4740 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077048 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-03-21 |
| Marketing End Date | 2014-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077048 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-22 |
| Marketing End Date | 2015-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA077048 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-22 |
| Marketing End Date | 2015-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA077048 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-22 |
| Marketing End Date | 2015-11-30 |