Package 43063-739-90

Brand: doxazosin

Generic: doxazosin
NDC Package

Package Facts

Identity

Package NDC 43063-739-90
Digits Only 4306373990
Product NDC 43063-739
Product ID 43063-739_414b2f15-260c-42cb-e063-6394a90a5225
Description

90 TABLET in 1 BOTTLE, PLASTIC (43063-739-90)

Marketing

Marketing Status
Marketed Since 2017-01-31
Brand doxazosin
Generic doxazosin
Sample Package No

Linked Drug Pages (1)

Doxazosin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "414b2f15-260c-42cb-e063-6394a90a5225", "openfda": {"upc": ["0343063739907"], "unii": ["86P6PQK0MU"], "rxcui": ["197626"], "spl_set_id": ["2ea9bb6b-a4f0-496a-b27b-4454167a4b70"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-739-90)", "package_ndc": "43063-739-90", "marketing_start_date": "20170131"}], "brand_name": "Doxazosin", "product_id": "43063-739_414b2f15-260c-42cb-e063-6394a90a5225", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "43063-739", "generic_name": "Doxazosin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxazosin", "active_ingredients": [{"name": "DOXAZOSIN MESYLATE", "strength": "2 mg/1"}], "application_number": "ANDA075580", "marketing_category": "ANDA", "marketing_start_date": "20110714", "listing_expiration_date": "20261231"}