cetirizine hydrochloride
Generic: cetirizine hydrochloride
Labeler: aurohealth llcDrug Facts
Product Profile
Brand Name
cetirizine hydrochloride
Generic Name
cetirizine hydrochloride
Labeler
aurohealth llc
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
cetirizine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58602-838
Product ID
58602-838_ef1f5185-9a05-4092-9bdc-954102616ccb
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA213557
Listing Expiration
2026-12-31
Marketing Start
2020-09-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58602838
Hyphenated Format
58602-838
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 (source: ndc)
Generic Name
cetirizine hydrochloride (source: ndc)
Application Number
ANDA213557 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 11 BLISTER PACK in 1 CARTON (58602-838-14) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
- 20 BLISTER PACK in 1 CARTON (58602-838-19) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
- 2 BLISTER PACK in 1 CARTON (58602-838-75) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
- 4 BLISTER PACK in 1 CARTON (58602-838-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
Packages (4)
58602-838-14
11 BLISTER PACK in 1 CARTON (58602-838-14) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
58602-838-19
20 BLISTER PACK in 1 CARTON (58602-838-19) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
58602-838-75
2 BLISTER PACK in 1 CARTON (58602-838-75) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
58602-838-76
4 BLISTER PACK in 1 CARTON (58602-838-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef1f5185-9a05-4092-9bdc-954102616ccb", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1011482"], "spl_set_id": ["17e93c22-1ff7-4af9-bd5a-448836aec65f"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "11 BLISTER PACK in 1 CARTON (58602-838-14) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)", "package_ndc": "58602-838-14", "marketing_start_date": "20200911"}, {"sample": false, "description": "20 BLISTER PACK in 1 CARTON (58602-838-19) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)", "package_ndc": "58602-838-19", "marketing_start_date": "20250128"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (58602-838-75) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)", "package_ndc": "58602-838-75", "marketing_start_date": "20200911"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (58602-838-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74)", "package_ndc": "58602-838-76", "marketing_start_date": "20200911"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "58602-838_ef1f5185-9a05-4092-9bdc-954102616ccb", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "58602-838", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213557", "marketing_category": "ANDA", "marketing_start_date": "20200911", "listing_expiration_date": "20261231"}