allergy relief

Generic: levocetirizine dihydrochloride

Labeler: albertsons companies
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name levocetirizine dihydrochloride
Labeler albertsons companies
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

levocetirizine dihydrochloride 5 mg/1

Manufacturer
Albertsons Companies

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
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21130732
Hyphenated Format 21130-732

Supplemental Identifiers

RxCUI
855172
UNII
SOD6A38AGA

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
  • 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
source: ndc

Packages (2)

Ingredients (1)

levocetirizine dihydrochloride (5 mg/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"}