doxazosin

Generic: doxazosin

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxazosin
Generic Name doxazosin
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxazosin mesylate 2 mg/1

Manufacturer
direct rx

Identifiers & Regulatory

Product NDC 72189-117
Product ID 72189-117_2be8ef13-7e70-fc50-e063-6394a90a0f27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202824
Listing Expiration 2026-12-31
Marketing Start 2020-12-02

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189117
Hyphenated Format 72189-117

Supplemental Identifiers

RxCUI
197626
UNII
86P6PQK0MU

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 doxazosin (source: ndc)
Generic Name doxazosin (source: ndc)
Application Number ANDA202824 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (72189-117-60)
source: ndc

Packages (1)

72189-117-60 60 TABLET in 1 BOTTLE (72189-117-60)

Ingredients (1)

doxazosin mesylate (2 mg/1)

Linked Drug Pages (1)

DOXAZOSIN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be8ef13-7e70-fc50-e063-6394a90a0f27", "openfda": {"unii": ["86P6PQK0MU"], "rxcui": ["197626"], "spl_set_id": ["b57cf33b-e0bd-54e9-e053-2a95a90a5a6a"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-117-60)", "package_ndc": "72189-117-60", "marketing_start_date": "20201202"}], "brand_name": "DOXAZOSIN", "product_id": "72189-117_2be8ef13-7e70-fc50-e063-6394a90a0f27", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72189-117", "generic_name": "DOXAZOSIN", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXAZOSIN", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "2 mg/1"}], "application_number": "ANDA202824", "marketing_category": "ANDA", "marketing_start_date": "20201202", "listing_expiration_date": "20261231"}