cetirizine hydrochloride 10 mg

Generic: cetirizine hydrochloride

Labeler: yyba corp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cetirizine hydrochloride 10 mg
Generic Name cetirizine hydrochloride
Labeler yyba corp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
YYBA CORP

Identifiers & Regulatory

Product NDC 73581-202
Product ID 73581-202_0e13664c-b422-d2fa-e063-6394a90a2d33
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209274
Listing Expiration 2026-12-31
Marketing Start 2021-06-16

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 73581202
Hyphenated Format 73581-202

Supplemental Identifiers

RxCUI
1014678
UNII
64O047KTOA

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 cetirizine hydrochloride 10 mg (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA209274 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (73581-202-01)
  • 500 TABLET in 1 BOTTLE (73581-202-05)
source: ndc

Packages (2)

73581-202-01 100 TABLET in 1 BOTTLE (73581-202-01) 73581-202-05 500 TABLET in 1 BOTTLE (73581-202-05)

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

CETIRIZINE HYDROCHLORIDE 10 MG ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e13664c-b422-d2fa-e063-6394a90a2d33", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["0502f197-21e1-44f2-b621-c8df1ccd956e"], "manufacturer_name": ["YYBA CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (73581-202-01)", "package_ndc": "73581-202-01", "marketing_start_date": "20210616"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (73581-202-05)", "package_ndc": "73581-202-05", "marketing_start_date": "20210617"}], "brand_name": "CETIRIZINE HYDROCHLORIDE 10 MG", "product_id": "73581-202_0e13664c-b422-d2fa-e063-6394a90a2d33", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "73581-202", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CETIRIZINE HYDROCHLORIDE", "brand_name_suffix": "10 MG", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20210616", "listing_expiration_date": "20261231"}