NDC 0603-0210 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-0210 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part332 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-03-12 |
| Marketing End Date | 2017-07-24 |