NDC 43598-225 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 43598-225 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA062216 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1979-08-02 |
| Marketing End Date | 2018-12-21 |
| Marketing Category | ANDA |
| Application Number | ANDA062216 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1979-08-02 |
| Marketing End Date | 2018-12-21 |