Package 45802-919-39

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45802-919-39
Digits Only 4580291939
Product NDC 45802-919
Description

1 BOTTLE in 1 CARTON (45802-919-39) / 30 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2008-10-15
Brand 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": "431bdf74-dfe3-4e4f-91e9-2b638ada6d47", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["91fe3ab8-c155-4482-9f06-f029d3563aad"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-919-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "45802-919-39", "marketing_start_date": "20081015"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-919-87)  / 300 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "45802-919-87", "marketing_start_date": "20071227"}], "brand_name": "cetirizine hydrochloride", "product_id": "45802-919_431bdf74-dfe3-4e4f-91e9-2b638ada6d47", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "45802-919", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "cetirizine hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20071227", "listing_expiration_date": "20261231"}