Package 0228-4241-06

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0228-4241-06
Digits Only 0228424106
Product NDC 0228-4241
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-4241-06)

Marketing

Marketing Status
Marketed Since 2015-06-17
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": "5082cfd3-e748-4c4b-81ba-0957f02244a5", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["0100c70d-7fde-46a1-8374-940550a27e43"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-4241-06)", "package_ndc": "0228-4241-06", "marketing_start_date": "20150617"}], "brand_name": "Clonidine Hydrochloride", "product_id": "0228-4241_5082cfd3-e748-4c4b-81ba-0957f02244a5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "0228-4241", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA203320", "marketing_category": "ANDA", "marketing_start_date": "20150617", "listing_expiration_date": "20261231"}