levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride

Labeler: walmart inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levocetirizine dihydrochloride
Generic Name levocetirizine dihydrochloride
Labeler walmart inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

levocetirizine dihydrochloride 5 mg/1

Manufacturer
Walmart Inc.

Identifiers & Regulatory

Product NDC 49035-492
Product ID 49035-492_faf3eee1-908d-7d25-bfaf-14c26daabcf7
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA210375
Listing Expiration 2027-12-31
Marketing Start 2019-07-26

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 49035492
Hyphenated Format 49035-492

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 levocetirizine dihydrochloride (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 (49035-492-10) / 10 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (49035-492-12) / 120 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 BOTTLE (49035-492-35) / 35 TABLET, COATED in 1 BOTTLE
  • 2 BLISTER PACK in 1 BLISTER PACK (49035-492-79) / 5 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (4)

49035-492-10 1 BOTTLE in 1 CARTON (49035-492-10) / 10 TABLET, COATED in 1 BOTTLE 49035-492-12 1 BOTTLE in 1 CARTON (49035-492-12) / 120 TABLET, COATED in 1 BOTTLE 49035-492-35 1 BOTTLE in 1 BOTTLE (49035-492-35) / 35 TABLET, COATED in 1 BOTTLE 49035-492-79 2 BLISTER PACK in 1 BLISTER PACK (49035-492-79) / 5 TABLET, COATED in 1 BLISTER PACK

Ingredients (1)

levocetirizine dihydrochloride (5 mg/1)

Linked Drug Pages (1)

Levocetirizine Dihydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "faf3eee1-908d-7d25-bfaf-14c26daabcf7", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["82da5fa1-3633-2c48-32b9-d15482f308a1"], "manufacturer_name": ["Walmart Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49035-492-10)  / 10 TABLET, COATED in 1 BOTTLE", "package_ndc": "49035-492-10", "marketing_start_date": "20260115"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (49035-492-12)  / 120 TABLET, COATED in 1 BOTTLE", "package_ndc": "49035-492-12", "marketing_start_date": "20260115"}, {"sample": false, "description": "1 BOTTLE in 1 BOTTLE (49035-492-35)  / 35 TABLET, COATED in 1 BOTTLE", "package_ndc": "49035-492-35", "marketing_start_date": "20190726"}, {"sample": false, "description": "2 BLISTER PACK in 1 BLISTER PACK (49035-492-79)  / 5 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "49035-492-79", "marketing_start_date": "20190726"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "49035-492_faf3eee1-908d-7d25-bfaf-14c26daabcf7", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "49035-492", "generic_name": "Levocetirizine Dihydrochloride", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Levocetirizine Dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210375", "marketing_category": "ANDA", "marketing_start_date": "20190726", "listing_expiration_date": "20271231"}