Package 70518-4141-0

{"route": ["ORAL"], "spl_id": "3a0b52a9-eb8c-08fe-e063-6394a90a6f9f", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["8f41912e-12ce-4174-a0fb-cfb4888d8d58"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4141-0)", "package_ndc": "70518-4141-0", "marketing_start_date": "20240716"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-1)", "package_ndc": "70518-4141-1", "marketing_start_date": "20250326"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-2)", "package_ndc": "70518-4141-2", "marketing_start_date": "20250715"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "70518-4141_3a0b52a9-eb8c-08fe-e063-6394a90a6f9f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-4141", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20240716", "listing_expiration_date": "20261231"}