Package 69848-006-09

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69848-006-09
Digits Only 6984800609
Product NDC 69848-006
Product ID 69848-006_468e40c3-a669-29bd-e063-6394a90a8812
Description

90 TABLET in 1 BOTTLE (69848-006-09)

Marketing

Marketing Status
Marketed Since 2021-06-30
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": "468e40c3-a669-29bd-e063-6394a90a8812", "openfda": {"upc": ["0813874020438"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["c8d711cd-7214-c7d5-e053-2995a90a6b67"], "manufacturer_name": ["Granules USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (69848-006-09)", "package_ndc": "69848-006-09", "marketing_start_date": "20210630"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "69848-006_468e40c3-a669-29bd-e063-6394a90a8812", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69848-006", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Granules USA, Inc.", "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": "20210630", "listing_expiration_date": "20261231"}