doxazosin

Generic: doxazosin

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxazosin
Generic Name doxazosin
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxazosin mesylate 1 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4272
Product ID 68071-4272_1a3da45c-c361-88c1-e063-6394a90a53ca
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202824
Listing Expiration 2026-12-31
Marketing Start 2015-03-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680714272
Hyphenated Format 68071-4272

Supplemental Identifiers

RxCUI
197625
UPC
0368071427233
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
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-4272-3)
source: ndc

Packages (1)

68071-4272-3 30 TABLET in 1 BOTTLE (68071-4272-3)

Ingredients (1)

doxazosin mesylate (1 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": "1a3da45c-c361-88c1-e063-6394a90a53ca", "openfda": {"upc": ["0368071427233"], "unii": ["86P6PQK0MU"], "rxcui": ["197625"], "spl_set_id": ["64a243e6-7056-115d-e053-2a91aa0a510f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4272-3)", "package_ndc": "68071-4272-3", "marketing_start_date": "20180207"}], "brand_name": "Doxazosin", "product_id": "68071-4272_1a3da45c-c361-88c1-e063-6394a90a53ca", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68071-4272", "generic_name": "Doxazosin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxazosin", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "1 mg/1"}], "application_number": "ANDA202824", "marketing_category": "ANDA", "marketing_start_date": "20150304", "listing_expiration_date": "20261231"}