NDC 49035-102 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49035-102 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part331 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-10-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph final |
Application Number | part331 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-16 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-04-11 |
Inactivation Date | 2019-10-29 |
Marketing Category | OTC monograph final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-04-07 |
Marketing Category | OTC monograph final |
Application Number | part331 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-22 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph final |
Application Number | part331 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-22 |
Inactivation Date | 2020-01-31 |