allergy relief
Generic: levocetirizine dihydrochloride
Labeler: yyba corpDrug Facts
Product Profile
Brand Name
allergy relief
Generic Name
levocetirizine dihydrochloride
Labeler
yyba corp
Dosage Form
TABLET
Routes
Active Ingredients
levocetirizine dihydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
73581-201
Product ID
73581-201_450fca8a-7ac1-d5fc-e063-6394a90aec36
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA213513
Listing Expiration
2026-12-31
Marketing Start
2020-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73581201
Hyphenated Format
73581-201
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA213513 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 1 BOTTLE in 1 BOX (73581-201-18) / 18 TABLET in 1 BOTTLE
- 1 BOTTLE in 1 BOX (73581-201-80) / 180 TABLET in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "450fca8a-7ac1-d5fc-e063-6394a90aec36", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["8ee69332-742d-4071-95df-84bc42e170e7"], "manufacturer_name": ["YYBA CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (73581-201-18) / 18 TABLET in 1 BOTTLE", "package_ndc": "73581-201-18", "marketing_start_date": "20251202"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (73581-201-80) / 180 TABLET in 1 BOTTLE", "package_ndc": "73581-201-80", "marketing_start_date": "20200630"}], "brand_name": "ALLERGY RELIEF", "product_id": "73581-201_450fca8a-7ac1-d5fc-e063-6394a90aec36", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "73581-201", "generic_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALLERGY RELIEF", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA213513", "marketing_category": "ANDA", "marketing_start_date": "20200630", "listing_expiration_date": "20261231"}