Package 70518-3554-2

{"route": ["ORAL"], "spl_id": "3d3126f1-bcb0-b2a9-e063-6294a90adc7e", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["d121146e-7439-4169-a421-dab7b882b8aa"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3554-0)", "package_ndc": "70518-3554-0", "marketing_start_date": "20221013"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-3554-1)", "package_ndc": "70518-3554-1", "marketing_start_date": "20230301"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3554-2)", "package_ndc": "70518-3554-2", "marketing_start_date": "20250823"}], "brand_name": "Fluoxetine", "product_id": "70518-3554_3d3126f1-bcb0-b2a9-e063-6294a90adc7e", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-3554", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20221013", "listing_expiration_date": "20261231"}