NDC 0078-0126 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0078-0126 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA019758 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1989-09-30 |
| Marketing End Date | 2014-02-28 |
| Marketing Category | NDA |
| Application Number | NDA019758 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1989-09-30 |
| Marketing End Date | 2017-03-31 |
| Marketing Category | NDA |
| Application Number | NDA019758 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1989-09-30 |
| Marketing End Date | 2017-03-31 |
| Marketing Category | NDA |
| Application Number | NDA019758 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-03-22 |
| Marketing End Date | 2017-03-31 |