Package 71610-123-60
Brand: cetirizine
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
71610-123-60
Digits Only
7161012360
Product NDC
71610-123
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-123-60)
Marketing
Marketing Status
Brand
cetirizine
Generic
cetirizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4528b1ee-ac82-2b33-e063-6294a90a599a", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["4a45672b-67d3-4739-86ec-0a6696dd83d4"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-123-60)", "package_ndc": "71610-123-60", "marketing_start_date": "20180817"}], "brand_name": "Cetirizine", "product_id": "71610-123_4528b1ee-ac82-2b33-e063-6294a90a599a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71610-123", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}