Package 42291-259-01

Brand: doxazosin

Generic: doxazosin
NDC Package

Package Facts

Identity

Package NDC 42291-259-01
Digits Only 4229125901
Product NDC 42291-259
Description

100 TABLET in 1 BOTTLE (42291-259-01)

Marketing

Marketing Status
Marketed Since 2015-04-09
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": "435672b7-4a90-85ba-e063-6394a90a2d63", "openfda": {"unii": ["86P6PQK0MU"], "rxcui": ["197626", "197627", "197628"], "spl_set_id": ["e3d381c1-3b2f-af70-f4e6-08d6202eed25"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42291-259-01)", "package_ndc": "42291-259-01", "marketing_start_date": "20150409"}], "brand_name": "Doxazosin", "product_id": "42291-259_435672b7-4a90-85ba-e063-6394a90a2d63", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "42291-259", "generic_name": "Doxazosin", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxazosin", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "4 mg/1"}], "application_number": "ANDA075580", "marketing_category": "ANDA", "marketing_start_date": "20150409", "listing_expiration_date": "20261231"}