cabinet allergy relief (68210-0119)

Drug Facts

Product Profile

Brand Name cabinet allergy relief

Generic Name cetirizine hydrochloride

Labeler spirit pharmaceutical llc

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer

Spirit Pharmaceutical LLC

Identifiers & Regulatory

Product NDC 68210-0119

Product ID 68210-0119_2a804c42-e22a-703e-e063-6394a90a3b1b

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209274

Listing Expiration 2026-12-31

Marketing Start 2019-10-25

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 682100119

Hyphenated Format 68210-0119

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 cabinet allergy relief (source: ndc)

Generic Name cetirizine hydrochloride (source: ndc)

Application Number ANDA209274 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

10 mg/1

source: ndc

Packaging

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0119-0)
300 TABLET, FILM COATED in 1 BOTTLE (68210-0119-1)
1 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

source: ndc

Packages (3)

68210-0119-0 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0119-0) 68210-0119-1 300 TABLET, FILM COATED in 1 BOTTLE (68210-0119-1) 68210-0119-3 1 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

CABINET Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "2a804c42-e22a-703e-e063-6394a90a3b1b", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["e49c3c91-aab8-478e-97fa-04ed06180021"], "manufacturer_name": ["Spirit Pharmaceutical LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0119-0)", "package_ndc": "68210-0119-0", "marketing_start_date": "20191025"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (68210-0119-1)", "package_ndc": "68210-0119-1", "marketing_start_date": "20200310"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3)  / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68210-0119-3", "marketing_start_date": "20200310"}], "brand_name": "CABINET Allergy Relief", "product_id": "68210-0119_2a804c42-e22a-703e-e063-6394a90a3b1b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68210-0119", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Spirit Pharmaceutical LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CABINET Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20191025", "listing_expiration_date": "20261231"}