Package 70436-041-01

Brand: guanfacine

Generic: guanfacine
NDC Package

Package Facts

Identity

Package NDC 70436-041-01
Digits Only 7043604101
Product NDC 70436-041
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-041-01)

Marketing

Marketing Status
Marketed Since 2022-08-01
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": "44e07739-2e64-f744-e063-6394a90ab3ac", "openfda": {"upc": ["0370436039012", "0370436042012", "0370436041015", "0370436040018"], "unii": ["PML56A160O"], "rxcui": ["862006", "862013", "862019", "862025"], "spl_set_id": ["ed65ca51-b9b0-43b9-9826-03a7be256a2a"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-041-01)", "package_ndc": "70436-041-01", "marketing_start_date": "20220801"}], "brand_name": "Guanfacine", "product_id": "70436-041_44e07739-2e64-f744-e063-6394a90ab3ac", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70436-041", "generic_name": "guanfacine", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA213428", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}