Package 63629-2318-1

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2318-1
Digits Only 6362923181
Product NDC 63629-2318
Description

500 TABLET in 1 BOTTLE (63629-2318-1)

Marketing

Marketing Status
Marketed Since 2020-07-01
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "318e88ca-7d05-41a0-904f-a97b933d53b4", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["1df79865-c028-45c7-8580-9908eec80979"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-2318-1)", "package_ndc": "63629-2318-1", "marketing_start_date": "20200701"}], "brand_name": "Clonidine Hydrochloride", "product_id": "63629-2318_318e88ca-7d05-41a0-904f-a97b933d53b4", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "63629-2318", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA202297", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}