NDC 69512-700 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 69512-700 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part348 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-08-01 |
Marketing End Date | 2015-08-19 |
Marketing Category | OTC monograph not final |
Application Number | part348 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-08-19 |
Inactivation Date | 2020-01-31 |