Package 70518-4239-0

{"route": ["ORAL"], "spl_id": "38f3e618-59de-4504-e063-6394a90afa55", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["53a7e974-9945-4e42-8395-b567bf9f1c4e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4239-0)", "package_ndc": "70518-4239-0", "marketing_start_date": "20241213"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-1)", "package_ndc": "70518-4239-1", "marketing_start_date": "20250225"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-2)", "package_ndc": "70518-4239-2", "marketing_start_date": "20250619"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3)", "package_ndc": "70518-4239-3", "marketing_start_date": "20250701"}], "brand_name": "escitalopram", "product_id": "70518-4239_38f3e618-59de-4504-e063-6394a90afa55", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4239", "generic_name": "escitalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20241213", "listing_expiration_date": "20261231"}