NDC 16729-212 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16729-212 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA202824 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-04-29 |
| Marketing End Date | 2018-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA202824 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-07-26 |
| Marketing End Date | 2018-10-31 |