NDC 0406-1772 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0406-1772 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA075738 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-08 | 
| Marketing End Date | 2009-08-20 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075738 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-08 | 
| Marketing End Date | 2011-07-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075738 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-08 | 
| Marketing End Date | 2011-07-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075738 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-08 | 
| Marketing End Date | 2011-07-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075738 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-08 | 
| Marketing End Date | 2011-07-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075738 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-08 | 
| Marketing End Date | 2009-08-20 |