Package 83939-0003-0

Brand: cetirizine

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 83939-0003-0
Digits Only 8393900030
Product NDC 83939-0003
Description

50 POUCH in 1 BOX, UNIT-DOSE (83939-0003-0) / 1 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2025-11-03
Brand cetirizine
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43f4168a-615f-a724-e063-6394a90a24b6", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["43f40b92-f0e0-8808-e063-6394a90a656b"], "manufacturer_name": ["VERITYRX, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (83939-0003-0)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "83939-0003-0", "marketing_start_date": "20251103"}, {"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (83939-0003-2)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "83939-0003-2", "marketing_start_date": "20251103"}, {"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (83939-0003-3)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "83939-0003-3", "marketing_start_date": "20251103"}], "brand_name": "Cetirizine", "product_id": "83939-0003_43f4168a-615f-a724-e063-6394a90a24b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "83939-0003", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "VERITYRX, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20251103", "listing_expiration_date": "20261231"}