NDC 70518-3495
Doxepin
Doxepin
Doxepin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Doxepin Hydrochloride.
| Product ID | 70518-3495_e6fda530-b5c7-5955-e053-2995a90a97cf |
| NDC | 70518-3495 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Doxepin |
| Generic Name | Doxepin |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2022-08-23 |
| Marketing Category | ANDA / |
| Application Number | ANDA201951 |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DOXEPIN HYDROCHLORIDE |
| Active Ingredient Strength | 6 mg/1 |
| Pharm Classes | Tricyclic Antidepressant [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |