NDC 0093-0149 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-0149 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074201 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-11 |
| Marketing End Date | 2012-02-29 |
| Marketing Category | ANDA |
| Application Number | ANDA074201 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-12-22 |
| Marketing End Date | 2017-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074201 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-12-22 |
| Marketing End Date | 2017-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074201 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-13 |
| Marketing End Date | 2018-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074201 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-12-22 |
| Marketing End Date | 2018-01-31 |