NDC 0555-0832 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0555-0832 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040145 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-07-25 |
| Marketing End Date | 2017-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA040145 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-07-25 |
| Marketing End Date | 2017-08-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040145 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-07-25 |
| Marketing End Date | 2010-03-28 |
| Marketing Category | ANDA |
| Application Number | ANDA040145 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-07-25 |
| Marketing End Date | 2010-03-28 |