doxepin

Generic: doxepin hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin
Generic Name doxepin hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxepin hydrochloride 3 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2474
Product ID 72162-2474_da27842d-9d36-4b4b-abbe-da72f998e300
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202510
Listing Expiration 2026-12-31
Marketing Start 2022-09-12

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622474
Hyphenated Format 72162-2474

Supplemental Identifiers

RxCUI
966787
UNII
3U9A0FE9N5

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 (source: ndc)
Generic Name doxepin hydrochloride (source: ndc)
Application Number ANDA202510 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72162-2474-3)
source: ndc

Packages (1)

72162-2474-3 30 TABLET in 1 BOTTLE (72162-2474-3)

Ingredients (1)

doxepin hydrochloride (3 mg/1)

Linked Drug Pages (1)

Doxepin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "da27842d-9d36-4b4b-abbe-da72f998e300", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787"], "spl_set_id": ["bc3b0401-df4a-46a2-a29b-3d70e72aa88b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2474-3)", "package_ndc": "72162-2474-3", "marketing_start_date": "20250501"}], "brand_name": "Doxepin", "product_id": "72162-2474_da27842d-9d36-4b4b-abbe-da72f998e300", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72162-2474", "generic_name": "doxepin hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA202510", "marketing_category": "ANDA", "marketing_start_date": "20220912", "listing_expiration_date": "20261231"}