NDC 67767-133 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67767-133 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA077455 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2008-03-26 | 
| Marketing End Date | 2015-02-28 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077455 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2008-03-26 | 
| Marketing End Date | 2015-07-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077455 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2008-03-26 | 
| Marketing End Date | 2015-09-30 |