cvs cetirizine hydrochloride

Generic: cetirizine hydrochloride

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cvs cetirizine hydrochloride
Generic Name cetirizine hydrochloride
Labeler cvs pharmacy
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
CVS Pharmacy

Identifiers & Regulatory

Product NDC 51316-182
Product ID 51316-182_3f168e67-2692-2005-e063-6394a90a747e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077829
Listing Expiration 2026-12-31
Marketing Start 2025-10-22

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 51316182
Hyphenated Format 51316-182

Supplemental Identifiers

RxCUI
1014678
UPC
0050428000311
UNII
64O047KTOA

Packaging Origin

Original Packager
true

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 cvs cetirizine hydrochloride (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA077829 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 365 TABLET in 1 BOTTLE (51316-182-10)
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": "3f168e67-2692-2005-e063-6394a90a747e", "openfda": {"upc": ["0050428000311"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["3d711302-dc4e-0a69-e063-6394a90ade10"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 BOTTLE (51316-182-10)", "package_ndc": "51316-182-10", "marketing_start_date": "20251022"}], "brand_name": "CVS Cetirizine Hydrochloride", "product_id": "51316-182_3f168e67-2692-2005-e063-6394a90a747e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51316-182", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}