Package 72162-2339-2
Brand: cetirizine hydrochloride
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
72162-2339-2
Digits Only
7216223392
Product NDC
72162-2339
Description
1 BOTTLE in 1 CARTON (72162-2339-2) / 118 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
cetirizine hydrochloride
Generic
cetirizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e6a15967-12aa-4d72-81ee-f2625b82c59d", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["0dc5a72f-1cc4-4cfc-a969-0ed781f7aa6f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72162-2339-2) / 118 mL in 1 BOTTLE", "package_ndc": "72162-2339-2", "marketing_start_date": "20240618"}], "brand_name": "cetirizine hydrochloride", "product_id": "72162-2339_e6a15967-12aa-4d72-81ee-f2625b82c59d", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72162-2339", "generic_name": "cetirizine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "cetirizine hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA090254", "marketing_category": "ANDA", "marketing_start_date": "20080415", "listing_expiration_date": "20261231"}