Package 72572-097-25

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "258b16e7-f7b5-45aa-b024-23743c3435a2", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["311659", "1743704"], "spl_set_id": ["2e6020f5-a486-41cc-8956-58b5f6751aa2"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72572-097-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72572-097-01)", "package_ndc": "72572-097-25", "marketing_start_date": "20251201"}], "brand_name": "Methylprednisolone Sodium Succinate", "product_id": "72572-097_258b16e7-f7b5-45aa-b024-23743c3435a2", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72572-097", "generic_name": "Methylprednisolone Sodium Succinate", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone Sodium Succinate", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "40 mg/1"}], "application_number": "ANDA203125", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}