NDC 0172-2932 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-2932 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA070343 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-06-08 |
| Marketing End Date | 1993-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA070343 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1986-02-20 |
| Marketing End Date | 1993-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA070343 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1986-02-20 |
| Marketing End Date | 1993-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA070343 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1986-02-20 |
| Marketing End Date | 1993-07-31 |