allergy relief
Generic: levocetirizine dihydrochloride
Labeler: albertsons companiesDrug Facts
Product Profile
Brand Name
allergy relief
Generic Name
levocetirizine dihydrochloride
Labeler
albertsons companies
Dosage Form
TABLET, COATED
Routes
Active Ingredients
levocetirizine dihydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
21130-732
Product ID
21130-732_f2d46324-71b9-4ac8-839d-bb2fa3c04a48
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA210375
Listing Expiration
2027-12-31
Marketing Start
2018-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130732
Hyphenated Format
21130-732
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (21130-732-10) / 5 TABLET, COATED in 1 BLISTER PACK
- 1 BOTTLE in 1 CARTON (21130-732-35) / 35 TABLET, COATED 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": "f2d46324-71b9-4ac8-839d-bb2fa3c04a48", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["e1a6932b-d076-6573-5b88-7b06c3a91681"], "manufacturer_name": ["Albertsons Companies"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (21130-732-10) / 5 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "21130-732-10", "marketing_start_date": "20180630"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-732-35) / 35 TABLET, COATED in 1 BOTTLE", "package_ndc": "21130-732-35", "marketing_start_date": "20180630"}], "brand_name": "Allergy Relief", "product_id": "21130-732_f2d46324-71b9-4ac8-839d-bb2fa3c04a48", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "21130-732", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Albertsons Companies", "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": "20180630", "listing_expiration_date": "20271231"}