NDC 0472-3901 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0472-3901 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073085 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2014-04-09 |
| Marketing End Date | 2017-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA073085 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2014-04-09 |
| Marketing End Date | 2017-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA073085 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2014-04-09 |
| Marketing End Date | 2017-11-30 |