zyrtec allergy

Generic: cetirizine hydrochloride

Labeler: redpharm drug inc
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zyrtec allergy
Generic Name cetirizine hydrochloride
Labeler redpharm drug inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
RedPharm Drug Inc

Identifiers & Regulatory

Product NDC 67296-1484
Product ID 67296-1484_2c62c754-9699-47f7-e063-6294a90a94fe
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA019835
Listing Expiration 2026-12-31
Marketing Start 2008-01-01

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 672961484
Hyphenated Format 67296-1484

Supplemental Identifiers

RxCUI
1014678 1020026
UPC
0312547204361
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
  • 30 TABLET, FILM COATED in 1 BOTTLE (67296-1484-3)
source: ndc

Packages (1)

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

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"}