NDC 0591-5787 is a Capsule in the Bulk Ingredient category. It is labeled and distributed by Actavis Pharma, Inc..
| Product ID | 0591-5787_4c73f701-c78c-4d78-a7b0-aa6c7674c778 |
| NDC | 0591-5787 |
| Product Type | Bulk Ingredient |
| Proprietary Name | NDC 0591-5787 |
| Dosage Form | Capsule |
| Marketing Start Date | 1992-07-01 |
| Marketing Category | / DRUG FOR FURTHER PROCESSING |
| Labeler Name | Actavis Pharma, Inc. |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA073554 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-07-01 |
| Marketing End Date | 2017-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073554 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-06-02 |
| Marketing End Date | 2013-05-09 |
| Marketing Category | ANDA |
| Application Number | ANDA073554 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-07-01 |
| Marketing End Date | 2017-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073554 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-07-01 |
| Marketing End Date | 2018-02-28 |
| Ingredient | Strength |
|---|---|
| NORTRIPTYLINE HYDROCHLORIDE | 25 mg/1 |