Package 72162-1801-1

Brand: guanfacine

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 72162-1801-1
Digits Only 7216218011
Product NDC 72162-1801
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1801-1)

Marketing

Marketing Status
Marketed Since 2018-08-17
Brand guanfacine
Generic guanfacine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "50c35259-c035-46e9-bfb1-ff5121e6aec4", "openfda": {"unii": ["PML56A160O"], "rxcui": ["862025"], "spl_set_id": ["c20cc7eb-9de5-407a-8943-c4d2e3f78444"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1801-1)", "package_ndc": "72162-1801-1", "marketing_start_date": "20180817"}], "brand_name": "Guanfacine", "product_id": "72162-1801_50c35259-c035-46e9-bfb1-ff5121e6aec4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "72162-1801", "generic_name": "Guanfacine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA205689", "marketing_category": "ANDA", "marketing_start_date": "20180817", "listing_expiration_date": "20261231"}