Package 70518-4342-0

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4342-0
Digits Only 7051843420
Product NDC 70518-4342
Description

30 TABLET in 1 BOTTLE, PLASTIC (70518-4342-0)

Marketing

Marketing Status
Marketed Since 2025-05-18
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": "35bb250a-9f02-c3dc-e063-6394a90a87e7", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["00c6d67a-bb11-4884-9eeb-4e1b8701a08b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4342-0)", "package_ndc": "70518-4342-0", "marketing_start_date": "20250518"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4342-1)", "package_ndc": "70518-4342-1", "marketing_start_date": "20250519"}], "brand_name": "Clonidine Hydrochloride", "product_id": "70518-4342_35bb250a-9f02-c3dc-e063-6394a90a87e7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-4342", "generic_name": "Clonidine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA070974", "marketing_category": "ANDA", "marketing_start_date": "20250518", "listing_expiration_date": "20261231"}