Package 53329-652-38

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53329-652-38
Digits Only 5332965238
Product NDC 53329-652
Product ID 53329-652_efd12ec8-8f3d-c1e3-e053-2995a90a685a
Description

90 TABLET in 1 BOTTLE (53329-652-38)

Marketing

Marketing Status
Marketed Since 2007-12-27
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cetirizine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "efd12ec8-8f3d-c1e3-e053-2995a90a685a", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["6823d475-84c6-4d9f-838d-925ccfb96c97"], "manufacturer_name": ["Medline Industries, LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (53329-652-38)", "package_ndc": "53329-652-38", "marketing_start_date": "20071227"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "53329-652_efd12ec8-8f3d-c1e3-e053-2995a90a685a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "53329-652", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Medline Industries, LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077498", "marketing_category": "ANDA", "marketing_start_date": "20071227", "listing_expiration_date": "20261231"}