Package 50090-6538-3

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6538-3
Digits Only 5009065383
Product NDC 50090-6538
Description

90 TABLET, COATED in 1 BOTTLE (50090-6538-3)

Marketing

Marketing Status
Marketed Since 2023-07-05
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": "b6221e59-ed88-4d25-a948-0f90c16f8dcf", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["f4da9adf-840d-4526-86a6-6666183fd107"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50090-6538-1)", "package_ndc": "50090-6538-1", "marketing_start_date": "20230704"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-6538-3)", "package_ndc": "50090-6538-3", "marketing_start_date": "20230705"}], "brand_name": "Cetirizine hydrochloride", "product_id": "50090-6538_b6221e59-ed88-4d25-a948-0f90c16f8dcf", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-6538", "generic_name": "Cetirizine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}