Package 71205-484-90

{"route": ["ORAL"], "spl_id": "b27e3d0c-4d85-44fa-bd4e-6210e8b5dcab", "openfda": {"upc": ["0371205484309"], "unii": ["33067B3N2M"], "rxcui": ["312748"], "spl_set_id": ["1aafcf35-46cb-4a6f-81d4-821c599bdb71"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-484-30)", "package_ndc": "71205-484-30", "marketing_start_date": "20201008"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-484-60)", "package_ndc": "71205-484-60", "marketing_start_date": "20201008"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-484-90)", "package_ndc": "71205-484-90", "marketing_start_date": "20201008"}], "brand_name": "QUINAPRIL", "product_id": "71205-484_b27e3d0c-4d85-44fa-bd4e-6210e8b5dcab", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71205-484", "generic_name": "quinapril", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUINAPRIL", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205823", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}