Package 68210-4219-1

Brand: allergy relief

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68210-4219-1
Digits Only 6821042191
Product NDC 68210-4219
Product ID 68210-4219_2a838f53-0e3c-3892-e063-6394a90a23d6
Description

120 TABLET, FILM COATED in 1 JAR (68210-4219-1)

Marketing

Marketing Status
Marketed Since 2022-11-14
Brand allergy relief
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Allergy Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a838f53-0e3c-3892-e063-6394a90a23d6", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["507df969-804c-4e95-bb42-c1224fce2b28"], "manufacturer_name": ["Spirit Pharmaceutical LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 JAR (68210-4219-1)", "package_ndc": "68210-4219-1", "marketing_start_date": "20221114"}], "brand_name": "Allergy Relief", "product_id": "68210-4219_2a838f53-0e3c-3892-e063-6394a90a23d6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68210-4219", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Spirit Pharmaceutical LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20221114", "listing_expiration_date": "20261231"}