NDC 0591-3746 is a Tablet, Film Coated in the Bulk Ingredient category. It is labeled and distributed by Actavis Pharma, Inc..
| Product ID | 0591-3746_6492ceb6-be0a-480a-b12b-ce3cc4e3f386 |
| NDC | 0591-3746 |
| Product Type | Bulk Ingredient |
| Proprietary Name | NDC 0591-3746 |
| Dosage Form | Tablet, Film Coated |
| Marketing Start Date | 2011-02-22 |
| Marketing Category | / DRUG FOR FURTHER PROCESSING |
| Labeler Name | Actavis Pharma, Inc. |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA091129 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-02-22 |
| Marketing End Date | 2012-07-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091129 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-05-19 |
| Marketing End Date | 2011-10-25 |
| Marketing Category | ANDA |
| Application Number | ANDA091129 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-02-22 |
| Marketing End Date | 2012-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA091129 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-02-22 |
| Marketing End Date | 2012-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA091129 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-08-21 |
| Marketing End Date | 2012-07-31 |
| Ingredient | Strength |
|---|---|
| LOSARTAN POTASSIUM | 50 mg/1 |