NDC 0603-3886 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-3886 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA040358 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2000-05-31 | 
| Marketing End Date | 2013-12-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA040358 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2000-05-31 | 
| Marketing End Date | 2013-12-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA040358 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2000-05-31 | 
| Marketing End Date | 2013-12-31 |