NDC 0904-5229 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0904-5229 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-01-09 |
Marketing End Date | 2013-03-12 |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-01-09 |
Marketing End Date | 2013-03-12 |