Package 70000-0047-1

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride allergy
NDC Package

Package Facts

Identity

Package NDC 70000-0047-1
Digits Only 7000000471
Product NDC 70000-0047
Product ID 70000-0047_5c5725c9-4879-424d-829c-44017284977a
Description

365 TABLET in 1 BOTTLE (70000-0047-1)

Marketing

Marketing Status
Marketed Since 2020-03-26
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride allergy
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": "5c5725c9-4879-424d-829c-44017284977a", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["0cab7aa8-ded3-46f1-b801-2663cc9b0173"], "manufacturer_name": ["LEADER/ CARDINAL HEALTH 110, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 BOTTLE (70000-0047-1)", "package_ndc": "70000-0047-1", "marketing_start_date": "20200326"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "70000-0047_5c5725c9-4879-424d-829c-44017284977a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70000-0047", "generic_name": "Cetirizine Hydrochloride Allergy", "labeler_name": "LEADER/ CARDINAL HEALTH 110, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090760", "marketing_category": "ANDA", "marketing_start_date": "20200326", "listing_expiration_date": "20261231"}