NDC 0093-1016 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-1016 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075189 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-06-15 |
| Marketing End Date | 2013-08-06 |
| Marketing Category | ANDA |
| Application Number | ANDA075189 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2001-09-26 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075189 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-12-21 |
| Marketing End Date | 2013-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075189 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-20 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075189 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-02-24 |
| Marketing End Date | 2017-12-31 |