Package 0093-2070-01

Brand: doxazosin

Generic: doxazosin mesylate
NDC Package

Package Facts

Identity

Package NDC 0093-2070-01
Digits Only 0093207001
Product NDC 0093-2070
Description

100 TABLET in 1 BOTTLE (0093-2070-01)

Marketing

Marketing Status
Marketed Since 2014-08-12
Brand doxazosin
Generic doxazosin mesylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "69a65fb3-443c-4b78-bb8b-9d8feff93fed", "openfda": {"upc": ["0300932069015", "0300932070011", "0300932068018", "0300932067011"], "unii": ["86P6PQK0MU"], "rxcui": ["197625", "197626", "197627", "197628"], "spl_set_id": ["0aaa68a7-f73b-46d8-860f-a76d96897489"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-2070-01)", "package_ndc": "0093-2070-01", "marketing_start_date": "20140812"}], "brand_name": "Doxazosin", "product_id": "0093-2070_69a65fb3-443c-4b78-bb8b-9d8feff93fed", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0093-2070", "generic_name": "Doxazosin Mesylate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxazosin", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "1 mg/1"}], "application_number": "ANDA075536", "marketing_category": "ANDA", "marketing_start_date": "20140806", "listing_expiration_date": "20261231"}