NDC 0603-3883 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-3883 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040157 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-09 |
| Marketing End Date | 2013-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040157 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-09 |
| Marketing End Date | 2013-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040157 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-04-12 |
| Marketing End Date | 2013-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040157 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-09 |
| Marketing End Date | 2013-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040157 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-04-12 |
| Marketing End Date | 2013-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040157 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-04-12 |
| Marketing End Date | 2013-12-31 |