Package 50090-6493-0

Brand: guanfacine extended-release

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 50090-6493-0
Digits Only 5009064930
Product NDC 50090-6493
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6493-0)

Marketing

Marketing Status
Marketed Since 2023-05-22
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": "22450f1d-9d74-467c-96a8-a8a3d6a59e68", "openfda": {"unii": ["PML56A160O"], "rxcui": ["862019"], "spl_set_id": ["07797c4a-a799-436b-a77c-a2861a811a99"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6493-0)", "package_ndc": "50090-6493-0", "marketing_start_date": "20230522"}], "brand_name": "Guanfacine extended-release", "product_id": "50090-6493_22450f1d-9d74-467c-96a8-a8a3d6a59e68", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "50090-6493", "generic_name": "guanfacine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine extended-release", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA205430", "marketing_category": "ANDA", "marketing_start_date": "20181003", "listing_expiration_date": "20261231"}