Search by Drug Name or NDC
NDC 42806-0531-10 Doxepin Hydrochloride 50 mg/1 Details
Doxepin Hydrochloride 50 mg/1
Doxepin Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Epic Pharma, LLC. The primary component is DOXEPIN HYDROCHLORIDE.
Product Information
| NDC | 42806-0531 |
|---|---|
| Product ID | 42806-531_baef2304-82cb-41cc-b671-51b3b7886f55 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Doxepin Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Doxepin Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | DOXEPIN HYDROCHLORIDE |
| Labeler Name | Epic Pharma, LLC |
| Pharmaceutical Class | Tricyclic Antidepressant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA210675 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 42806-0531-10 (42806053110)
| NDC Package Code | 42806-531-10 |
|---|---|
| Billing NDC | 42806053110 |
| Package | 1000 CAPSULE in 1 BOTTLE (42806-531-10) |
| Marketing Start Date | 2022-03-03 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |