NDC 63874-201 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63874-201 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074843 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-01 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | ANDA |
| Application Number | ANDA074843 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-01 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | ANDA |
| Application Number | ANDA074843 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-01 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | ANDA |
| Application Number | ANDA074843 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-01 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | ANDA |
| Application Number | ANDA074843 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-01 |
| Inactivation Date | 2019-10-21 |