NDC 0603-0855 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-0855 |
Marketing Category | / |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1995-04-01 |
Marketing End Date | 2018-03-31 |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 1995-04-01 |
Marketing End Date | 2018-03-31 |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 1995-04-01 |
Marketing End Date | 2018-03-31 |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1995-04-01 |
Marketing End Date | 2018-03-31 |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 1995-04-01 |
Marketing End Date | 2018-03-31 |