zyrtec allergy

Generic: cetirizine hydrochloride

Labeler: navajo manufacturing company incorporated
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zyrtec allergy
Generic Name cetirizine hydrochloride
Labeler navajo manufacturing company incorporated
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Navajo Manufacturing Company Incorporated

Identifiers & Regulatory

Product NDC 67751-192
Product ID 67751-192_f70c23f1-f2a8-8415-e053-6394a90a64dc
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA019835
Listing Expiration 2026-12-31
Marketing Start 2019-11-20

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67751192
Hyphenated Format 67751-192

Supplemental Identifiers

RxCUI
1014678 1020026
UNII
64O047KTOA

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zyrtec allergy (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number NDA019835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 POUCH in 1 CARTON (67751-192-01) / 1 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (1)

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

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Zyrtec Allergy ndc-match (0.9)

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"}