NDC 45802-361 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 45802-361 |
Marketing Category | / |
Marketing Category | NDA authorized generic |
Application Number | NDA017522 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2006-01-05 |
Marketing End Date | 2015-12-31 |
Marketing Category | NDA authorized generic |
Application Number | NDA017522 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2006-01-05 |
Marketing End Date | 2015-12-31 |