Package 66267-464-90

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66267-464-90
Digits Only 6626746490
Product NDC 66267-464
Description

90 TABLET in 1 BOTTLE, PLASTIC (66267-464-90)

Marketing

Marketing Status
Marketed Since 2016-11-15
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": "1fa6f6ca-cf68-49fd-e063-6394a90a73f2", "openfda": {"upc": ["0366267464307"], "unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["415b168c-1267-2777-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (66267-464-90)", "package_ndc": "66267-464-90", "marketing_start_date": "20161115"}], "brand_name": "clonidine hydrochloride", "product_id": "66267-464_1fa6f6ca-cf68-49fd-e063-6394a90a73f2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "66267-464", "generic_name": "clonidine hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}