Package 0615-8479-39

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8479-39
Digits Only 0615847939
Product NDC 0615-8479
Product ID 0615-8479_1125df7c-ba82-46fe-a411-05322146a3b9
Description

30 TABLET, COATED in 1 BLISTER PACK (0615-8479-39)

Marketing

Marketing Status
Marketed Since 2023-07-31
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cetirizine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1125df7c-ba82-46fe-a411-05322146a3b9", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["b53d5e8a-a30c-4025-aa72-d2776a112e3e"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (0615-8479-39)", "package_ndc": "0615-8479-39", "marketing_start_date": "20230731"}], "brand_name": "Cetirizine hydrochloride", "product_id": "0615-8479_1125df7c-ba82-46fe-a411-05322146a3b9", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0615-8479", "generic_name": "Cetirizine hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}