NDC 16590-266 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-266 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA070974 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1986-12-16 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA070974 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1986-12-16 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA070974 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1986-12-16 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA070974 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 1986-12-16 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA070974 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1986-12-16 | 
| Inactivation Date | 2019-10-21 |