doxazosin

Generic: doxazosin

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxazosin
Generic Name doxazosin
Labeler apotex corp.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxazosin mesylate 8 mg/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-0096
Product ID 60505-0096_7e2e0788-60a4-f586-7ece-7b27d5068dc8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075580
Listing Expiration 2026-12-31
Marketing Start 2011-07-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605050096
Hyphenated Format 60505-0096

Supplemental Identifiers

RxCUI
197625 197626 197627 197628
UPC
0360505009503 0360505009602 0360505009305 0360505009404
UNII
86P6PQK0MU

Packaging Origin

Original Packager
true

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
  • 100 TABLET in 1 BOTTLE (60505-0096-0)
  • 1000 TABLET in 1 BOTTLE (60505-0096-1)
source: ndc

Packages (2)

60505-0096-0 100 TABLET in 1 BOTTLE (60505-0096-0) 60505-0096-1 1000 TABLET in 1 BOTTLE (60505-0096-1)

Ingredients (1)

doxazosin mesylate (8 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": "7e2e0788-60a4-f586-7ece-7b27d5068dc8", "openfda": {"upc": ["0360505009503", "0360505009602", "0360505009305", "0360505009404"], "unii": ["86P6PQK0MU"], "rxcui": ["197625", "197626", "197627", "197628"], "spl_set_id": ["4fa5c2f7-cda9-56cd-622f-b3d05dc7c94b"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-0096-0)", "package_ndc": "60505-0096-0", "marketing_start_date": "20110714"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (60505-0096-1)", "package_ndc": "60505-0096-1", "marketing_start_date": "20110714"}], "brand_name": "Doxazosin", "product_id": "60505-0096_7e2e0788-60a4-f586-7ece-7b27d5068dc8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60505-0096", "generic_name": "Doxazosin", "labeler_name": "Apotex Corp.", "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": "20110714", "listing_expiration_date": "20261231"}