NDC 67253-821 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67253-821 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA087068 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1980-11-05 |
| Marketing End Date | 2011-01-01 |
| Marketing Category | ANDA |
| Application Number | ANDA087068 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1980-11-05 |
| Marketing End Date | 2011-01-01 |
| Marketing Category | ANDA |
| Application Number | ANDA087068 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1980-11-05 |
| Marketing End Date | 2011-01-01 |
| Marketing Category | ANDA |
| Application Number | ANDA087068 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1980-11-05 |
| Marketing End Date | 2011-01-01 |