Package 67751-192-01

Brand: zyrtec allergy

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67751-192-01
Digits Only 6775119201
Product NDC 67751-192
Product ID 67751-192_f70c23f1-f2a8-8415-e053-6394a90a64dc
Description

1 POUCH in 1 CARTON (67751-192-01) / 1 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2019-11-20
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": "f70c23f1-f2a8-8415-e053-6394a90a64dc", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678", "1020026"], "spl_set_id": ["9c4693cb-f066-0666-e053-2a95a90a96d3"], "manufacturer_name": ["Navajo Manufacturing Company Incorporated"]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-192-01)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-192-01", "marketing_start_date": "20191120"}], "brand_name": "Zyrtec Allergy", "product_id": "67751-192_f70c23f1-f2a8-8415-e053-6394a90a64dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67751-192", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Navajo Manufacturing Company Incorporated", "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": "20191120", "listing_expiration_date": "20261231"}