Package 0904-5523-61

Brand: doxazosin

Generic: doxazosin
NDC Package

Package Facts

Identity

Package NDC 0904-5523-61
Digits Only 0904552361
Product NDC 0904-5523
Description

100 BLISTER PACK in 1 CARTON (0904-5523-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2011-07-14
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": "ec0e1a20-88d4-457b-88fa-eff3071d0b9f", "openfda": {"unii": ["86P6PQK0MU"], "rxcui": ["197625", "197626", "197627"], "spl_set_id": ["3354196f-bbcf-4bc5-94f6-e6e8e132acb1"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-5523-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-5523-61", "marketing_start_date": "20110714"}], "brand_name": "Doxazosin", "product_id": "0904-5523_ec0e1a20-88d4-457b-88fa-eff3071d0b9f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0904-5523", "generic_name": "Doxazosin", "labeler_name": "Major Pharmaceuticals", "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"}