doxepin hcl

Generic: doxepin hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hcl
Generic Name doxepin hcl
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxepin hydrochloride 10 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-355
Product ID 72189-355_2c4c85cc-c2b7-ac98-e063-6294a90a973c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213063
Listing Expiration 2026-12-31
Marketing Start 2022-05-10

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189355
Hyphenated Format 72189-355

Supplemental Identifiers

RxCUI
1000048
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 hcl (source: ndc)
Generic Name doxepin hcl (source: ndc)
Application Number ANDA213063 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72189-355-30)
source: ndc

Packages (1)

72189-355-30 30 CAPSULE in 1 BOTTLE (72189-355-30)

Ingredients (1)

doxepin hydrochloride (10 mg/1)

Linked Drug Pages (1)

Doxepin HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4c85cc-c2b7-ac98-e063-6294a90a973c", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["dea965fe-6b54-bbf0-e053-2a95a90a1003"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-355-30)", "package_ndc": "72189-355-30", "marketing_start_date": "20220510"}], "brand_name": "Doxepin HCL", "product_id": "72189-355_2c4c85cc-c2b7-ac98-e063-6294a90a973c", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-355", "generic_name": "Doxepin HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin HCL", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213063", "marketing_category": "ANDA", "marketing_start_date": "20220510", "listing_expiration_date": "20261231"}