cetirizine hydrochloride
Generic: cetirizine hydrochloride
Labeler: bajaj medical, llcDrug Facts
Product Profile
Brand Name
cetirizine hydrochloride
Generic Name
cetirizine hydrochloride
Labeler
bajaj medical, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
cetirizine hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
61037-479
Product ID
61037-479_3b5908fd-b2c0-ba45-e063-6294a90a6fb0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090191
Listing Expiration
2026-12-31
Marketing Start
2023-09-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61037479
Hyphenated Format
61037-479
Supplemental Identifiers
RxCUI
UPC
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
ANDA090191 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 240 mL in 1 BOTTLE, PLASTIC (61037-479-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b5908fd-b2c0-ba45-e063-6294a90a6fb0", "openfda": {"upc": ["0361037479048"], "unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["3b5908f1-faba-c317-e063-6294a90aa8a7"], "manufacturer_name": ["BAJAJ MEDICAL, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE, PLASTIC (61037-479-04)", "package_ndc": "61037-479-04", "marketing_start_date": "20250606"}], "brand_name": "CETIRIZINE HYDROCHLORIDE", "product_id": "61037-479_3b5908fd-b2c0-ba45-e063-6294a90a6fb0", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "61037-479", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "BAJAJ MEDICAL, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CETIRIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA090191", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20261231"}