Package 70518-2009-0

{"route": ["ORAL"], "spl_id": "498bd99f-a4a0-0498-e063-6394a90a73cc", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["9LHU78OQFD"], "rxcui": ["197904"], "spl_set_id": ["ff040b3c-6790-40d7-bd64-a4073b4a2045"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2009-0)", "package_ndc": "70518-2009-0", "marketing_start_date": "20190411"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2009-1)", "package_ndc": "70518-2009-1", "marketing_start_date": "20211026"}], "brand_name": "Lovastatin", "product_id": "70518-2009_498bd99f-a4a0-0498-e063-6394a90a73cc", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-2009", "generic_name": "lovastatin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "20 mg/1"}], "application_number": "ANDA078296", "marketing_category": "ANDA", "marketing_start_date": "20190411", "listing_expiration_date": "20271231"}