Package 68788-4072-9

{"route": ["ORAL"], "spl_id": "a462f9c0-45ef-49b1-b0d8-a02a75a4b731", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["a462f9c0-45ef-49b1-b0d8-a02a75a4b731"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68788-4072-3)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "68788-4072-3", "marketing_start_date": "20260127"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-4072-6)", "package_ndc": "68788-4072-6", "marketing_start_date": "20260127"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-4072-9)", "package_ndc": "68788-4072-9", "marketing_start_date": "20260127"}], "brand_name": "cetirizine hydrochloride", "product_id": "68788-4072_a462f9c0-45ef-49b1-b0d8-a02a75a4b731", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68788-4072", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "cetirizine hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20260127", "listing_expiration_date": "20271231"}