doxepin hydrochloride

Generic: doxepin hydrochloride

Labeler: currax pharmaceuticals llc dba cypress, hawthorn, macoven
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler currax pharmaceuticals llc dba cypress, hawthorn, macoven
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxepin hydrochloride 3 mg/1

Manufacturer
Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven

Identifiers & Regulatory

Product NDC 44183-103
Product ID 44183-103_db184464-82a3-4710-a6aa-6a1c437a7bfc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022036
Listing Expiration 2026-12-31
Marketing Start 2010-08-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 44183103
Hyphenated Format 44183-103

Supplemental Identifiers

RxCUI
966787 966793
UNII
3U9A0FE9N5

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name doxepin hydrochloride (source: ndc)
Generic Name doxepin hydrochloride (source: ndc)
Application Number NDA022036 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (44183-103-30)
source: ndc

Packages (1)

Ingredients (1)

doxepin hydrochloride (3 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "db184464-82a3-4710-a6aa-6a1c437a7bfc", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["5b4dba99-6b66-4091-94f1-bf5f021c688a"], "manufacturer_name": ["Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (44183-103-30)", "package_ndc": "44183-103-30", "marketing_start_date": "20100801"}], "brand_name": "doxepin hydrochloride", "product_id": "44183-103_db184464-82a3-4710-a6aa-6a1c437a7bfc", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "44183-103", "generic_name": "doxepin hydrochloride", "labeler_name": "Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "NDA022036", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20100801", "listing_expiration_date": "20261231"}