NDC 49884-407 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49884-407 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA019962 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-07-26 |
| Marketing End Date | 2016-11-30 |
| Marketing Category | NDA authorized generic |
| Application Number | NDA019962 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-07-26 |
| Marketing End Date | 2016-11-30 |