NDC 0009-5135 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0009-5135 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021130 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-04-18 |
Marketing End Date | 2018-07-31 |
Marketing Category | NDA |
Application Number | NDA021130 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-04-18 |
Marketing End Date | 2018-02-28 |
Marketing Category | NDA |
Application Number | NDA021130 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2000-04-18 |
Marketing End Date | 2018-07-31 |