allergy relief

Generic: cetirizine hydrochloride

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name cetirizine hydrochloride
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-4101
Product ID 0363-4101_28f9d48e-60ee-4d58-af55-0b6206044e31
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078336
Listing Expiration 2026-12-31
Marketing Start 2021-10-21

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 03634101
Hyphenated Format 0363-4101

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 allergy relief (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA078336 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-4101-39) / 30 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-4101-47) / 150 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-4101-58) / 40 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-4101-72) / 60 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-4101-75) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-4101-88) / 365 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-4101-95) / 45 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (7)

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": "28f9d48e-60ee-4d58-af55-0b6206044e31", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["678dcc09-55da-4d9d-a39a-c450c61c387b"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-4101-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-4101-39", "marketing_start_date": "20211206"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-4101-47)  / 150 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-4101-47", "marketing_start_date": "20220502"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-4101-58)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-4101-58", "marketing_start_date": "20241213"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-4101-72)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-4101-72", "marketing_start_date": "20220617"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-4101-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-4101-75", "marketing_start_date": "20211021"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-4101-88)  / 365 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-4101-88", "marketing_start_date": "20220308"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-4101-95)  / 45 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-4101-95", "marketing_start_date": "20220325"}], "brand_name": "allergy relief", "product_id": "0363-4101_28f9d48e-60ee-4d58-af55-0b6206044e31", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-4101", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "allergy relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20211021", "listing_expiration_date": "20261231"}