NDC 36800-829 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 36800-829 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-09-09 |
Marketing End Date | 2015-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-09-23 |
Marketing End Date | 2015-10-21 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-09-08 |
Marketing End Date | 2015-09-16 |