NDC 0228-3315
Doxepin
Doxepin
Doxepin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Actavis Pharma, Inc.. The primary component is Doxepin Hydrochloride.
| Product ID | 0228-3315_4e2dbdb6-3855-46e1-8379-b88434176323 |
| NDC | 0228-3315 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Doxepin |
| Generic Name | Doxepin |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2020-01-02 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA201951 |
| Labeler Name | Actavis Pharma, Inc. |
| Substance Name | DOXEPIN HYDROCHLORIDE |
| Active Ingredient Strength | 3 mg/1 |
| Pharm Classes | Tricyclic Antidepressant [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |