allergy relief

Generic: levocetirizine dihydrochloride

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

Drug Facts

Product Profile

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

levocetirizine dihydrochloride 5 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-3901
Product ID 0363-3901_9f9913a7-9054-4d73-b480-e9a5f6446373
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211983
Listing Expiration 2026-12-31
Marketing Start 2021-09-23

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 03633901
Hyphenated Format 0363-3901

Supplemental Identifiers

RxCUI
855172
UNII
SOD6A38AGA

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 levocetirizine dihydrochloride (source: ndc)
Application Number ANDA211983 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-3901-01) / 35 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-3901-27) / 80 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-3901-76) / 120 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

0363-3901-01 1 BOTTLE in 1 CARTON (0363-3901-01) / 35 TABLET, FILM COATED in 1 BOTTLE 0363-3901-27 1 BOTTLE in 1 CARTON (0363-3901-27) / 80 TABLET, FILM COATED in 1 BOTTLE 0363-3901-76 1 BOTTLE in 1 CARTON (0363-3901-76) / 120 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

levocetirizine dihydrochloride (5 mg/1)

Linked Drug Pages (1)

allergy relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9f9913a7-9054-4d73-b480-e9a5f6446373", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["5033f8e3-c1c4-44e9-a774-703d9b04e82c"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-3901-01)  / 35 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-3901-01", "marketing_start_date": "20210923"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-3901-27)  / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-3901-27", "marketing_start_date": "20210923"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-3901-76)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-3901-76", "marketing_start_date": "20210923"}], "brand_name": "allergy relief", "product_id": "0363-3901_9f9913a7-9054-4d73-b480-e9a5f6446373", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-3901", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "allergy relief", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211983", "marketing_category": "ANDA", "marketing_start_date": "20210923", "listing_expiration_date": "20261231"}