NDC 11026-2681 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 11026-2681 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 2007-10-01 |
Inactivation Date | 2019-11-13 |