NDC 63481-229 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63481-229 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA022239 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2015-06-08 |
Marketing End Date | 2017-05-31 |
Marketing Category | NDA |
Application Number | NDA022239 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-06-08 |
Marketing End Date | 2017-05-31 |
Marketing Category | NDA |
Application Number | NDA022239 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2015-06-08 |
Marketing End Date | 2017-05-31 |
Marketing Category | NDA |
Application Number | NDA022239 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-06-08 |
Marketing End Date | 2017-05-31 |