NDC 42549-537 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42549-537 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA076017 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-09 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA076017 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2009-06-09 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA076017 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-09 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA076017 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-09 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA076017 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-06-09 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA076017 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2009-06-09 | 
| Inactivation Date | 2019-11-13 |