Package 72319-019-04

Brand: guanfacine

Generic: gaunfacine
NDC Package

Package Facts

Identity

Package NDC 72319-019-04
Digits Only 7231901904
Product NDC 72319-019
Product ID 72319-019_262d9624-c761-8f3d-e063-6394a90a2640
Description

100 TABLET in 1 BOTTLE (72319-019-04)

Marketing

Marketing Status
Marketed Since 2022-10-31
Brand guanfacine
Generic gaunfacine
Sample Package No

Linked Drug Pages (1)

Guanfacine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "262d9624-c761-8f3d-e063-6394a90a2640", "openfda": {"upc": ["0372319019043", "0372319018046"], "unii": ["PML56A160O"], "rxcui": ["197745", "197746"], "spl_set_id": ["387b33dd-829d-4dab-afe4-078fd1559027"], "manufacturer_name": ["i3 Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72319-019-04)", "package_ndc": "72319-019-04", "marketing_start_date": "20221031"}], "brand_name": "Guanfacine", "product_id": "72319-019_262d9624-c761-8f3d-e063-6394a90a2640", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "72319-019", "generic_name": "Gaunfacine", "labeler_name": "i3 Pharmaceuticals, LLC", "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": "20221031", "listing_expiration_date": "20261231"}