Package 37835-611-14

{"route": ["ORAL"], "spl_id": "36d0b7f3-2156-873a-e063-6294a90ac015", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["cbb270c3-34a4-4af8-9da0-2e545787cb55"], "manufacturer_name": ["Bi-Mar"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (37835-611-14)", "package_ndc": "37835-611-14", "marketing_start_date": "20250501"}, {"sample": false, "description": "35 TABLET in 1 BOTTLE (37835-611-35)", "package_ndc": "37835-611-35", "marketing_start_date": "20250501"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (37835-611-90)", "package_ndc": "37835-611-90", "marketing_start_date": "20250501"}], "brand_name": "Cetirizine hydrochloride", "product_id": "37835-611_36d0b7f3-2156-873a-e063-6294a90ac015", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37835-611", "generic_name": "Cetirizine hydrochloride", "labeler_name": "Bi-Mar", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}