NDC 63777-214 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63777-214 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-04-19 |
| Marketing End Date | 2014-01-27 |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-07-02 |
| Marketing End Date | 2015-02-17 |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-04-19 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-04-19 |
| Marketing End Date | 2014-01-27 |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-04-19 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-04-19 |
| Marketing End Date | 2014-01-27 |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-04-19 |
| Marketing End Date | 2014-01-27 |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-04-19 |
| Marketing End Date | 2014-01-27 |