NDC 67253-141 is a in the category. It is labeled and distributed by Dava Pharmaceuticals, Inc..
| Product ID | 67253-141_dfbf89a1-4e62-4322-835d-10e59469c095 |
| NDC | 67253-141 |
| Proprietary Name | NDC 67253-141 |
| Marketing Start Date | 1988-02-25 |
| Marketing Category | / |
| Labeler Name | DAVA Pharmaceuticals, Inc. |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA062881 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1988-02-25 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA062881 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1988-02-25 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA062881 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-09-29 |
| Marketing End Date | 2018-04-30 |
| Ingredient | Strength |
|---|---|
| AMOXICILLIN | 500 mg/1 |