Package 73141-019-04

Brand: guanfacine

Generic: gaunfacine
NDC Package

Package Facts

Identity

Package NDC 73141-019-04
Digits Only 7314101904
Product NDC 73141-019
Description

100 TABLET in 1 BOTTLE (73141-019-04)

Marketing

Marketing Status
Marketed Since 2025-04-08
Brand guanfacine
Generic gaunfacine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32c1e44a-6ccf-c3c7-e063-6394a90ad7fc", "openfda": {"unii": ["PML56A160O"], "rxcui": ["197745", "197746"], "spl_set_id": ["00c3b4d2-fc4d-4e68-9157-eb29d927deaf"], "manufacturer_name": ["A2A Integrated Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (73141-019-04)", "package_ndc": "73141-019-04", "marketing_start_date": "20250408"}], "brand_name": "Guanfacine", "product_id": "73141-019_32c1e44a-6ccf-c3c7-e063-6394a90ad7fc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "73141-019", "generic_name": "Gaunfacine", "labeler_name": "A2A Integrated Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA216828", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}