Package 0615-2574-39

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-2574-39
Digits Only 0615257439
Product NDC 0615-2574
Description

30 TABLET in 1 BLISTER PACK (0615-2574-39)

Marketing

Marketing Status
Marketed Since 2019-02-07
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": "69be47b6-270c-4e24-9352-560a5b5b250f", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["acdddd91-ffe3-4b9b-9c59-0328e018b662"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-2574-39)", "package_ndc": "0615-2574-39", "marketing_start_date": "20190207"}], "brand_name": "Clonidine Hydrochloride", "product_id": "0615-2574_69be47b6-270c-4e24-9352-560a5b5b250f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "0615-2574", "generic_name": "Clonidine Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA070976", "marketing_category": "ANDA", "marketing_start_date": "19950103", "listing_expiration_date": "20261231"}