Package 70518-4335-0

{"route": ["ORAL"], "spl_id": "37757eb7-5206-9c45-e063-6294a90a4d99", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["bdc0c228-797a-42dd-8114-aa68c1eb3300"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4335-0)", "package_ndc": "70518-4335-0", "marketing_start_date": "20250501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4335-1)", "package_ndc": "70518-4335-1", "marketing_start_date": "20250601"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4335-2)", "package_ndc": "70518-4335-2", "marketing_start_date": "20250613"}], "brand_name": "Citalopram", "product_id": "70518-4335_37757eb7-5206-9c45-e063-6294a90a4d99", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4335", "generic_name": "Citalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}