cetirizine hydrochloride

Generic: cetirizine hydrochloride

Labeler: family dollar services, inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cetirizine hydrochloride
Generic Name cetirizine hydrochloride
Labeler family dollar services, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
FAMILY DOLLAR SERVICES, INC

Identifiers & Regulatory

Product NDC 55319-939
Product ID 55319-939_65ed577d-07a6-40e5-bff5-26b9ec806f04
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077498
Listing Expiration 2026-12-31
Marketing Start 2017-09-01

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 55319939
Hyphenated Format 55319-939

Supplemental Identifiers

RxCUI
1014678
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 cetirizine hydrochloride (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA077498 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (55319-939-30)
  • 14 TABLET in 1 BLISTER PACK (55319-939-54)
source: ndc

Packages (2)

55319-939-30 30 TABLET in 1 BOTTLE (55319-939-30) 55319-939-54 14 TABLET in 1 BLISTER PACK (55319-939-54)

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Cetirizine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "65ed577d-07a6-40e5-bff5-26b9ec806f04", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["b326dacc-6123-47a7-9fde-6909db1d780b"], "manufacturer_name": ["FAMILY DOLLAR SERVICES, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (55319-939-30)", "package_ndc": "55319-939-30", "marketing_start_date": "20170901"}, {"sample": false, "description": "14 TABLET in 1 BLISTER PACK (55319-939-54)", "package_ndc": "55319-939-54", "marketing_start_date": "20170901"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "55319-939_65ed577d-07a6-40e5-bff5-26b9ec806f04", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55319-939", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "FAMILY DOLLAR SERVICES, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077498", "marketing_category": "ANDA", "marketing_start_date": "20170901", "listing_expiration_date": "20261231"}