NDC 0172-5032 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-5032 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075776 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2012-12-07 |
| Marketing Category | ANDA |
| Application Number | ANDA075776 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2017-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA075776 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2012-12-07 |
| Marketing Category | ANDA |
| Application Number | ANDA075776 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2016-10-31 |