Package 67296-1484-3

Brand: zyrtec allergy

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-1484-3
Digits Only 6729614843
Product NDC 67296-1484
Product ID 67296-1484_2c62c754-9699-47f7-e063-6294a90a94fe
Description

30 TABLET, FILM COATED in 1 BOTTLE (67296-1484-3)

Marketing

Marketing Status
Marketed Since 2008-01-01
Brand zyrtec allergy
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Zyrtec Allergy ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c62c754-9699-47f7-e063-6294a90a94fe", "openfda": {"upc": ["0312547204361"], "unii": ["64O047KTOA"], "rxcui": ["1014678", "1020026"], "spl_set_id": ["f4c1f9fd-2d32-71d3-e053-2a95a90a3ba4"], "manufacturer_name": ["RedPharm Drug Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-1484-3)", "package_ndc": "67296-1484-3", "marketing_start_date": "20080101"}], "brand_name": "Zyrtec Allergy", "product_id": "67296-1484_2c62c754-9699-47f7-e063-6294a90a94fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67296-1484", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "RedPharm Drug Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zyrtec Allergy", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA019835", "marketing_category": "NDA", "marketing_start_date": "20080101", "listing_expiration_date": "20261231"}