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 72189-388
Product ID 72189-388_2c4cd5ef-e1b3-b248-e063-6394a90a540d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215483
Listing Expiration 2026-12-31
Marketing Start 2022-10-19

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189388
Hyphenated Format 72189-388

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 ANDA215483 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72189-388-30)
source: ndc

Packages (1)

72189-388-30 30 CAPSULE in 1 BOTTLE (72189-388-30)

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": "2c4cd5ef-e1b3-b248-e063-6394a90a540d", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["eb643108-7ae2-f476-e053-2995a90ab148"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-388-30)", "package_ndc": "72189-388-30", "marketing_start_date": "20221019"}], "brand_name": "Doxepin HCL", "product_id": "72189-388_2c4cd5ef-e1b3-b248-e063-6394a90a540d", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-388", "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": "ANDA215483", "marketing_category": "ANDA", "marketing_start_date": "20221019", "listing_expiration_date": "20261231"}