Package 65862-374-10

{"route": ["ORAL"], "spl_id": "a61e5c0a-ac35-4233-b852-5764350f60a1", "openfda": {"upc": ["0365862373014"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["d5fbc8ce-bd41-4bd0-b413-0dea97e596c3"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-374-01)", "package_ndc": "65862-374-01", "marketing_start_date": "20120911"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-374-05)", "package_ndc": "65862-374-05", "marketing_start_date": "20120911"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-374-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-374-10", "marketing_start_date": "20120911"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-374-30)", "package_ndc": "65862-374-30", "marketing_start_date": "20120911"}, {"sample": false, "description": "5000 TABLET, FILM COATED in 1 BOTTLE (65862-374-59)", "package_ndc": "65862-374-59", "marketing_start_date": "20120911"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-374-90)", "package_ndc": "65862-374-90", "marketing_start_date": "20120911"}], "brand_name": "Escitalopram", "product_id": "65862-374_a61e5c0a-ac35-4233-b852-5764350f60a1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-374", "generic_name": "Escitalopram Oxalate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}