NDC 0093-1039 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-1039 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075435 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2004-10-08 |
| Marketing End Date | 2010-01-20 |
| Marketing Category | ANDA |
| Application Number | ANDA075435 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2004-10-08 |
| Marketing End Date | 2010-01-20 |
| Marketing Category | ANDA |
| Application Number | ANDA075435 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-07-11 |
| Marketing End Date | 2010-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075435 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-10-08 |
| Marketing End Date | 2014-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075435 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-20 |
| Marketing End Date | 2014-08-31 |