NDC 0093-1042 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-1042 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075452 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-01-30 |
| Marketing End Date | 2014-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075452 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-01-30 |
| Marketing End Date | 2012-07-21 |
| Marketing Category | ANDA |
| Application Number | ANDA075452 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-01-30 |
| Marketing End Date | 2014-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075452 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-01-30 |
| Marketing End Date | 2012-07-21 |