Package 70518-4379-0

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4379-0
Digits Only 7051843790
Product NDC 70518-4379
Product ID 70518-4379_38f1df00-4f89-0e69-e063-6394a90a52ea
Description

60 TABLET in 1 BOTTLE, PLASTIC (70518-4379-0)

Marketing

Marketing Status
Marketed Since 2025-07-01
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38f1df00-4f89-0e69-e063-6394a90a52ea", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["6d7cfb02-e580-4658-a2fe-2149b515d434"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-4379-0)", "package_ndc": "70518-4379-0", "marketing_start_date": "20250701"}], "brand_name": "Clonidine Hydrochloride", "product_id": "70518-4379_38f1df00-4f89-0e69-e063-6394a90a52ea", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-4379", "generic_name": "Clonidine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20250701", "listing_expiration_date": "20261231"}