NDC 43598-222 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 43598-222 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA062226 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1979-09-19 |
| Marketing End Date | 2018-12-21 |
| Marketing Category | ANDA |
| Application Number | ANDA062226 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1979-09-19 |
| Marketing End Date | 2018-12-21 |
| Marketing Category | ANDA |
| Application Number | ANDA062226 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1979-09-19 |
| Marketing End Date | 2018-12-21 |