allergy relief

Generic: levocetirizine dihydrochloride

Labeler: amerisourcebergen drug corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name levocetirizine dihydrochloride
Labeler amerisourcebergen drug corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

levocetirizine dihydrochloride 5 mg/1

Manufacturer
AMERISOURCEBERGEN DRUG CORPORATION

Identifiers & Regulatory

Product NDC 46122-531
Product ID 46122-531_7dc5bf93-f17c-3267-33d9-f123f53c072b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA210375
Listing Expiration 2026-12-31
Marketing Start 2018-04-20

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 46122531
Hyphenated Format 46122-531

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 ANDA210375 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (46122-531-05) / 35 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (46122-531-61) / 80 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (2)

46122-531-05 1 BOTTLE in 1 CARTON (46122-531-05) / 35 TABLET, COATED in 1 BOTTLE 46122-531-61 1 BOTTLE in 1 CARTON (46122-531-61) / 80 TABLET, 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": "7dc5bf93-f17c-3267-33d9-f123f53c072b", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["fdf54de3-16a9-3b28-b4c4-d745322b3d3c"], "manufacturer_name": ["AMERISOURCEBERGEN DRUG CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46122-531-05)  / 35 TABLET, COATED in 1 BOTTLE", "package_ndc": "46122-531-05", "marketing_start_date": "20180420"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (46122-531-61)  / 80 TABLET, COATED in 1 BOTTLE", "package_ndc": "46122-531-61", "marketing_start_date": "20230901"}], "brand_name": "Allergy Relief", "product_id": "46122-531_7dc5bf93-f17c-3267-33d9-f123f53c072b", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "46122-531", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "AMERISOURCEBERGEN DRUG CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210375", "marketing_category": "ANDA", "marketing_start_date": "20180420", "listing_expiration_date": "20261231"}