Package 73581-202-05

Brand: cetirizine hydrochloride 10 mg

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 73581-202-05
Digits Only 7358120205
Product NDC 73581-202
Product ID 73581-202_0e13664c-b422-d2fa-e063-6394a90a2d33
Description

500 TABLET in 1 BOTTLE (73581-202-05)

Marketing

Marketing Status
Marketed Since 2021-06-17
Brand cetirizine hydrochloride 10 mg
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

CETIRIZINE HYDROCHLORIDE 10 MG ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e13664c-b422-d2fa-e063-6394a90a2d33", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["0502f197-21e1-44f2-b621-c8df1ccd956e"], "manufacturer_name": ["YYBA CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (73581-202-01)", "package_ndc": "73581-202-01", "marketing_start_date": "20210616"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (73581-202-05)", "package_ndc": "73581-202-05", "marketing_start_date": "20210617"}], "brand_name": "CETIRIZINE HYDROCHLORIDE 10 MG", "product_id": "73581-202_0e13664c-b422-d2fa-e063-6394a90a2d33", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "73581-202", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CETIRIZINE HYDROCHLORIDE", "brand_name_suffix": "10 MG", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20210616", "listing_expiration_date": "20261231"}