doxepin hydrochloride

Generic: doxepin hydrochloride

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

Drug Facts

Product Profile

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

doxepin hydrochloride 75 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2228
Product ID 72162-2228_aed9708c-54a5-4b76-b137-4cfcb47e89c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213474
Listing Expiration 2026-12-31
Marketing Start 2021-05-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622228
Hyphenated Format 72162-2228

Supplemental Identifiers

RxCUI
1000097
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 hydrochloride (source: ndc)
Generic Name doxepin hydrochloride (source: ndc)
Application Number ANDA213474 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (72162-2228-1)
source: ndc

Packages (1)

Ingredients (1)

doxepin hydrochloride (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aed9708c-54a5-4b76-b137-4cfcb47e89c9", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000097"], "spl_set_id": ["a4c804e3-4706-48d8-b928-b22c2dcaeed8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2228-1)", "package_ndc": "72162-2228-1", "marketing_start_date": "20240126"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72162-2228_aed9708c-54a5-4b76-b137-4cfcb47e89c9", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72162-2228", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA213474", "marketing_category": "ANDA", "marketing_start_date": "20210501", "listing_expiration_date": "20261231"}