NDC 57664-136 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 57664-136 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA040865 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-12-29 | 
| Marketing End Date | 2018-03-02 | 
| Marketing Category | ANDA | 
| Application Number | ANDA040865 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-12-29 | 
| Marketing End Date | 2018-03-02 | 
| Marketing Category | ANDA | 
| Application Number | ANDA040865 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2009-12-29 | 
| Marketing End Date | 2018-03-02 |