Package 60760-863-30

Brand: guanfacine

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 60760-863-30
Digits Only 6076086330
Product NDC 60760-863
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-863-30)

Marketing

Marketing Status
Marketed Since 2025-05-19
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": "35d3c939-2305-3f43-e063-6394a90afb4e", "openfda": {"unii": ["PML56A160O"], "rxcui": ["862006"], "spl_set_id": ["35d3c996-1755-c017-e063-6294a90abc1f"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-863-30)", "package_ndc": "60760-863-30", "marketing_start_date": "20250519"}], "brand_name": "GUANFACINE", "product_id": "60760-863_35d3c939-2305-3f43-e063-6394a90afb4e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "60760-863", "generic_name": "GUANFACINE", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GUANFACINE", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA217269", "marketing_category": "ANDA", "marketing_start_date": "20230808", "listing_expiration_date": "20261231"}