Package 68071-3811-6

Brand: doxazosin

Generic: doxazosin
NDC Package

Package Facts

Identity

Package NDC 68071-3811-6
Digits Only 6807138116
Product NDC 68071-3811
Description

60 TABLET in 1 BOTTLE (68071-3811-6)

Marketing

Marketing Status
Marketed Since 2025-03-19
Brand doxazosin
Generic doxazosin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30b6f043-d418-812c-e063-6294a90ad442", "openfda": {"upc": ["0368071381160"], "unii": ["86P6PQK0MU"], "rxcui": ["197626"], "spl_set_id": ["30b709d6-c438-c721-e063-6294a90abd61"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3811-6)", "package_ndc": "68071-3811-6", "marketing_start_date": "20250319"}], "brand_name": "Doxazosin", "product_id": "68071-3811_30b6f043-d418-812c-e063-6294a90ad442", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3811", "generic_name": "Doxazosin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxazosin", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "2 mg/1"}], "application_number": "ANDA208719", "marketing_category": "ANDA", "marketing_start_date": "20170831", "listing_expiration_date": "20261231"}