Package 10267-3579-1

Brand: cetirizine hydrochloride 10 mg

Generic: cetirizine hydrochloride 10 mg
NDC Package

Package Facts

Identity

Package NDC 10267-3579-1
Digits Only 1026735791
Product NDC 10267-3579
Description

1 BOTTLE in 1 CARTON (10267-3579-1) / 100 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-12-31
Brand cetirizine hydrochloride 10 mg
Generic cetirizine hydrochloride 10 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3633ac85-4814-e6a7-e063-6294a90a375d", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["84459f11-3405-4a8e-be38-333b7de2a578"], "manufacturer_name": ["Contract Pharmacal Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (10267-3579-1)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "10267-3579-1", "marketing_start_date": "20251231"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (10267-3579-3)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "10267-3579-3", "marketing_start_date": "20251231"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10267-3579-4)", "package_ndc": "10267-3579-4", "marketing_start_date": "20250531"}, {"sample": false, "description": "365 TABLET, FILM COATED in 1 BOTTLE (10267-3579-6)", "package_ndc": "10267-3579-6", "marketing_start_date": "20250416"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (10267-3579-7)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "10267-3579-7", "marketing_start_date": "20251231"}], "brand_name": "Cetirizine Hydrochloride 10 mg", "product_id": "10267-3579_3633ac85-4814-e6a7-e063-6294a90a375d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "10267-3579", "generic_name": "Cetirizine Hydrochloride 10 mg", "labeler_name": "Contract Pharmacal Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride 10 mg", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076047", "marketing_category": "ANDA", "marketing_start_date": "20250416", "listing_expiration_date": "20261231"}