Package 71335-2852-1

Brand: guanfacine extended-release

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 71335-2852-1
Digits Only 7133528521
Product NDC 71335-2852
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2852-1)

Marketing

Marketing Status
Marketed Since 2025-10-30
Brand guanfacine extended-release
Generic guanfacine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d2293e0c-0dd5-4024-89b1-826f81fe532c", "openfda": {"unii": ["PML56A160O"], "rxcui": ["862013"], "spl_set_id": ["178b649f-8c0f-4fea-a168-3ce4ff52129d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2852-1)", "package_ndc": "71335-2852-1", "marketing_start_date": "20251030"}], "brand_name": "Guanfacine extended-release", "product_id": "71335-2852_d2293e0c-0dd5-4024-89b1-826f81fe532c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71335-2852", "generic_name": "guanfacine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine extended-release", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA205430", "marketing_category": "ANDA", "marketing_start_date": "20181003", "listing_expiration_date": "20261231"}