Package 51316-182-10

Brand: cvs cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51316-182-10
Digits Only 5131618210
Product NDC 51316-182
Description

365 TABLET in 1 BOTTLE (51316-182-10)

Marketing

Marketing Status
Marketed Since 2025-10-22
Brand cvs cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f168e67-2692-2005-e063-6394a90a747e", "openfda": {"upc": ["0050428000311"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["3d711302-dc4e-0a69-e063-6394a90ade10"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 BOTTLE (51316-182-10)", "package_ndc": "51316-182-10", "marketing_start_date": "20251022"}], "brand_name": "CVS Cetirizine Hydrochloride", "product_id": "51316-182_3f168e67-2692-2005-e063-6394a90a747e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51316-182", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}