Package 70436-042-01
Brand: guanfacine
Generic: guanfacinePackage Facts
Identity
Package NDC
70436-042-01
Digits Only
7043604201
Product NDC
70436-042
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-042-01)
Marketing
Marketing Status
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 (70436-042-01)", "package_ndc": "70436-042-01", "marketing_start_date": "20220801"}], "brand_name": "Guanfacine", "product_id": "70436-042_44e07739-2e64-f744-e063-6394a90ab3ac", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70436-042", "generic_name": "guanfacine", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA213428", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}