Package 63629-8161-1

Brand: guanfacine

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 63629-8161-1
Digits Only 6362981611
Product NDC 63629-8161
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8161-1)

Marketing

Marketing Status
Marketed Since 2019-07-02
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": "846438f0-3355-4455-a7e8-f0db48bc6162", "openfda": {"unii": ["PML56A160O"], "rxcui": ["862006"], "spl_set_id": ["f070a54a-2738-4ef2-a98a-f9e7a7a56f55"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8161-1)", "package_ndc": "63629-8161-1", "marketing_start_date": "20190702"}], "brand_name": "Guanfacine", "product_id": "63629-8161_846438f0-3355-4455-a7e8-f0db48bc6162", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "63629-8161", "generic_name": "Guanfacine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA205689", "marketing_category": "ANDA", "marketing_start_date": "20180817", "listing_expiration_date": "20261231"}