NDC 0406-0357 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0406-0357 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA089160 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-04-22 | 
| Marketing End Date | 2017-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA089160 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-04-22 | 
| Marketing End Date | 2017-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA089160 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-02-09 | 
| Marketing End Date | 2017-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA089160 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2012-11-14 | 
| Marketing End Date | 2016-04-20 | 
| Marketing Category | ANDA | 
| Application Number | ANDA089160 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-04-22 | 
| Marketing End Date | 2017-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA089160 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2013-09-16 | 
| Marketing End Date | 2017-09-30 |