doxazosin

Generic: doxazosin

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

doxazosin mesylate 8 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-225
Product ID 50268-225_47e34870-0256-c99d-e063-6394a90ae59a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075580
Listing Expiration 2027-12-31
Marketing Start 2022-05-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268225
Hyphenated Format 50268-225

Supplemental Identifiers

RxCUI
197625 197626 197627 197628
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 ANDA075580 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-225-15) / 1 TABLET in 1 BLISTER PACK (50268-225-11)
source: ndc

Packages (1)

Ingredients (1)

doxazosin mesylate (8 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e34870-0256-c99d-e063-6394a90ae59a", "openfda": {"unii": ["86P6PQK0MU"], "rxcui": ["197625", "197626", "197627", "197628"], "spl_set_id": ["de9ab9a4-d8b8-8b36-e053-2a95a90aaa35"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-225-15)  / 1 TABLET in 1 BLISTER PACK (50268-225-11)", "package_ndc": "50268-225-15", "marketing_start_date": "20220509"}], "brand_name": "Doxazosin", "product_id": "50268-225_47e34870-0256-c99d-e063-6394a90ae59a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "50268-225", "generic_name": "Doxazosin", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxazosin", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "8 mg/1"}], "application_number": "ANDA075580", "marketing_category": "ANDA", "marketing_start_date": "20220509", "listing_expiration_date": "20271231"}