NDC 49884-685 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49884-685 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA070581 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 1985-10-17 | 
| Marketing End Date | 2019-01-23 | 
| Marketing Category | ANDA | 
| Application Number | ANDA070581 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 1985-10-17 | 
| Marketing End Date | 2019-01-23 |