Package 46708-497-30

{"route": ["ORAL"], "spl_id": "a4f0715d-590f-4b13-bb72-19cdca95aa01", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["27f70e15-ee22-47ae-ba87-20e2b4a1a4d6"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (46708-497-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "46708-497-10", "marketing_start_date": "20230124"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-497-30)", "package_ndc": "46708-497-30", "marketing_start_date": "20230124"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (46708-497-71)", "package_ndc": "46708-497-71", "marketing_start_date": "20230124"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (46708-497-90)", "package_ndc": "46708-497-90", "marketing_start_date": "20230124"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-497-91)", "package_ndc": "46708-497-91", "marketing_start_date": "20230124"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "46708-497_a4f0715d-590f-4b13-bb72-19cdca95aa01", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "46708-497", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA213248", "marketing_category": "ANDA", "marketing_start_date": "20230124", "listing_expiration_date": "20261231"}