Package 70518-4031-0

Brand: doxazosin

Generic: doxazosin
NDC Package

Package Facts

Identity

Package NDC 70518-4031-0
Digits Only 7051840310
Product NDC 70518-4031
Product ID 70518-4031_3f91d970-6366-7b75-e063-6394a90a77be
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4031-0)

Marketing

Marketing Status
Marketed Since 2024-02-28
Brand doxazosin
Generic doxazosin
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f91d970-6366-7b75-e063-6394a90a77be", "openfda": {"unii": ["86P6PQK0MU"], "rxcui": ["197627"], "spl_set_id": ["bf2f7b41-f14d-4fcd-8db3-f507ca6ff78b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4031-0)", "package_ndc": "70518-4031-0", "marketing_start_date": "20240228"}], "brand_name": "Doxazosin", "product_id": "70518-4031_3f91d970-6366-7b75-e063-6394a90a77be", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4031", "generic_name": "Doxazosin", "labeler_name": "REMEDYREPACK INC.", "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": "20240228", "listing_expiration_date": "20261231"}