Package 24979-199-01

Brand: guanfacine hydrochloride

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 24979-199-01
Digits Only 2497919901
Product NDC 24979-199
Description

100 TABLET in 1 BOTTLE (24979-199-01)

Marketing

Marketing Status
Marketed Since 2022-09-01
Brand guanfacine hydrochloride
Generic guanfacine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef3592ef-2184-43de-9f37-062bd24079d6", "openfda": {"upc": ["0324979199016", "0324979198019"], "unii": ["PML56A160O"], "rxcui": ["197745", "197746"], "spl_set_id": ["a0c2d95d-805c-4c7d-9733-52073a65218a"], "manufacturer_name": ["TWi Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (24979-199-01)", "package_ndc": "24979-199-01", "marketing_start_date": "20220901"}], "brand_name": "Guanfacine Hydrochloride", "product_id": "24979-199_ef3592ef-2184-43de-9f37-062bd24079d6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "24979-199", "generic_name": "Guanfacine", "labeler_name": "TWi Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine Hydrochloride", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA216399", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}