NDC 0172-5663 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-5663 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075385 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-03-02 |
| Marketing End Date | 2012-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075385 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-08-26 |
| Marketing End Date | 2012-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075385 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-03-02 |
| Marketing End Date | 2012-03-16 |
| Marketing Category | ANDA |
| Application Number | ANDA075385 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-03-02 |
| Marketing End Date | 2012-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075385 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-03-02 |
| Marketing End Date | 2012-03-16 |
| Marketing Category | ANDA |
| Application Number | ANDA075385 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-03-02 |
| Marketing End Date | 2012-04-30 |