NDC 43598-223 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 43598-223 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA050760 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1999-04-15 |
| Marketing End Date | 2018-12-21 |
| Marketing Category | NDA |
| Application Number | NDA050760 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1999-04-15 |
| Marketing End Date | 2018-12-21 |
| Marketing Category | NDA |
| Application Number | NDA050760 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1999-04-15 |
| Marketing End Date | 2018-12-21 |