Package 70518-2203-1

Brand: clonidine hydrochloride

Generic: clonidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2203-1
Digits Only 7051822031
Product NDC 70518-2203
Product ID 70518-2203_49dd11b5-ebe1-4e53-e063-6394a90a675a
Description

30 TABLET in 1 BLISTER PACK (70518-2203-1)

Marketing

Marketing Status
Marketed Since 2023-03-15
Brand clonidine hydrochloride
Generic clonidine hydrochloride
Sample Package No

Linked Drug Pages (1)

clonidine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49dd11b5-ebe1-4e53-e063-6394a90a675a", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["e96ab74c-eedf-4d71-8a35-d5ec3daa7592"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2203-1)", "package_ndc": "70518-2203-1", "marketing_start_date": "20230315"}], "brand_name": "clonidine hydrochloride", "product_id": "70518-2203_49dd11b5-ebe1-4e53-e063-6394a90a675a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-2203", "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": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20190710", "listing_expiration_date": "20271231"}