Package 63629-4914-1

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-4914-1
Digits Only 6362949141
Product NDC 63629-4914
Product ID 63629-4914_3db925ae-d07d-4da4-9dab-155db44d75a0
Description

30 TABLET in 1 BOTTLE (63629-4914-1)

Marketing

Marketing Status
Marketed Since 2013-02-19
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": "3db925ae-d07d-4da4-9dab-155db44d75a0", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014676"], "spl_set_id": ["ddec7d64-ab3d-4ddd-9bcd-b7f4d2b46be7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-4914-1)", "package_ndc": "63629-4914-1", "marketing_start_date": "20130219"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "63629-4914_3db925ae-d07d-4da4-9dab-155db44d75a0", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63629-4914", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20091001", "listing_expiration_date": "20261231"}