Package 57483-190-14
Brand: cetirizine hydrochloride (allergy)
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
57483-190-14
Digits Only
5748319014
Product NDC
57483-190
Description
365 TABLET in 1 BOTTLE (57483-190-14)
Marketing
Marketing Status
Brand
cetirizine hydrochloride (allergy)
Generic
cetirizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "89db2c96-62f6-4e75-8f0d-321b44094c60", "openfda": {"upc": ["0357483002480"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["89db2c96-62f6-4e75-8f0d-321b44094c60"], "manufacturer_name": ["INNOVUS PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 BOTTLE (57483-190-14)", "package_ndc": "57483-190-14", "marketing_start_date": "20250428"}], "brand_name": "Cetirizine Hydrochloride (Allergy)", "product_id": "57483-190_89db2c96-62f6-4e75-8f0d-321b44094c60", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57483-190", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "INNOVUS PHARMACEUTICALS, INC.", "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": "20250428", "listing_expiration_date": "20261231"}