NDC 0713-0222 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0713-0222 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA089525 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1988-07-26 |
| Marketing End Date | 2015-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA089525 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1988-07-26 |
| Marketing End Date | 2015-02-28 |