Package 70518-4539-0

Brand: guanfacine

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 70518-4539-0
Digits Only 7051845390
Product NDC 70518-4539
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4539-0)

Marketing

Marketing Status
Marketed Since 2025-12-23
Brand guanfacine
Generic guanfacine
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4858f0eb-08c7-1a50-e063-6394a90a4c5b", "openfda": {"unii": ["PML56A160O"], "rxcui": ["862006"], "spl_set_id": ["145a191d-9049-4014-9c42-503fdde063dc"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4539-0)", "package_ndc": "70518-4539-0", "marketing_start_date": "20251223"}], "brand_name": "Guanfacine", "product_id": "70518-4539_4858f0eb-08c7-1a50-e063-6394a90a4c5b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-4539", "generic_name": "Guanfacine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA219033", "marketing_category": "ANDA", "marketing_start_date": "20251223", "listing_expiration_date": "20271231"}