cetirizine hydrochloride (allergy)
Generic: cetirizine hydrochloride
Labeler: aurohealth llcDrug Facts
Product Profile
Brand Name
cetirizine hydrochloride (allergy)
Generic Name
cetirizine hydrochloride
Labeler
aurohealth llc
Dosage Form
TABLET
Routes
Active Ingredients
cetirizine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58602-823
Product ID
58602-823_bd9c2a41-9024-46a4-87c6-7d6f5f1fafbf
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA090760
Listing Expiration
2026-12-31
Marketing Start
2015-08-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58602823
Hyphenated Format
58602-823
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
cetirizine hydrochloride (allergy) (source: ndc)
Generic Name
cetirizine hydrochloride (source: ndc)
Application Number
ANDA090760 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (58602-823-39) / 365 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bd9c2a41-9024-46a4-87c6-7d6f5f1fafbf", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["7d214cba-951d-464e-b37e-e83098944fe6"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-823-39) / 365 TABLET in 1 BOTTLE", "package_ndc": "58602-823-39", "marketing_start_date": "20150805"}], "brand_name": "Cetirizine Hydrochloride (Allergy)", "product_id": "58602-823_bd9c2a41-9024-46a4-87c6-7d6f5f1fafbf", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "58602-823", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride (Allergy)", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090760", "marketing_category": "ANDA", "marketing_start_date": "20150805", "listing_expiration_date": "20261231"}