NDC 0113-0368 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0113-0368 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1997-01-14 |
| Marketing End Date | 2015-12-29 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-14 |
| Marketing End Date | 2015-12-29 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1997-01-14 |
| Marketing End Date | 2013-11-06 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-14 |
| Marketing End Date | 2015-12-29 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1997-01-14 |
| Marketing End Date | 2015-12-29 |
| Marketing Category | ANDA |
| Application Number | ANDA074661 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-14 |
| Marketing End Date | 2015-12-29 |