cetirizine hydrochloride (allergy)
Generic: cetirizine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cetirizine hydrochloride (allergy)
Generic Name
cetirizine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
cetirizine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6170
Product ID
50090-6170_406f752b-552b-4c29-9ca8-4cbf82ad5ed6
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
500906170
Hyphenated Format
50090-6170
Supplemental Identifiers
RxCUI
UNII
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
- 48 BOTTLE in 1 CASE (50090-6170-0) / 30 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": "406f752b-552b-4c29-9ca8-4cbf82ad5ed6", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["42c9636f-07af-44a3-8d84-c11e1b57783a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "48 BOTTLE in 1 CASE (50090-6170-0) / 30 TABLET in 1 BOTTLE", "package_ndc": "50090-6170-0", "marketing_start_date": "20221013"}], "brand_name": "Cetirizine Hydrochloride (Allergy)", "product_id": "50090-6170_406f752b-552b-4c29-9ca8-4cbf82ad5ed6", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-6170", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}