doxazosin

Generic: doxazosin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxazosin
Generic Name doxazosin
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxazosin mesylate 1 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0701
Product ID 50090-0701_3fba2a6d-a770-467a-b7a5-5a1f33e5f662
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075580
Listing Expiration 2027-12-31
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 500900701
Hyphenated Format 50090-0701

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
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-0701-0)
source: ndc

Packages (1)

50090-0701-0 30 TABLET in 1 BOTTLE (50090-0701-0)

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": "3fba2a6d-a770-467a-b7a5-5a1f33e5f662", "openfda": {"unii": ["86P6PQK0MU"], "rxcui": ["197625", "197626", "197627", "197628"], "spl_set_id": ["bfea0b5b-9354-490f-88ff-008134077d24"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-0701-0)", "package_ndc": "50090-0701-0", "marketing_start_date": "20141128"}], "brand_name": "Doxazosin", "product_id": "50090-0701_3fba2a6d-a770-467a-b7a5-5a1f33e5f662", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "50090-0701", "generic_name": "Doxazosin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxazosin", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "1 mg/1"}], "application_number": "ANDA075580", "marketing_category": "ANDA", "marketing_start_date": "20110714", "listing_expiration_date": "20271231"}