Package 62332-071-25

{"route": ["INTRAVENOUS"], "spl_id": "db0264f6-5825-49a1-bb86-746ece155660", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["a9e5fac6-2db6-4311-a98b-eb3f0dde19d6"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (62332-071-01)  / 10 mL in 1 VIAL", "package_ndc": "62332-071-01", "marketing_start_date": "20250331"}, {"sample": false, "description": "10 VIAL in 1 CARTON (62332-071-10)  / 10 mL in 1 VIAL", "package_ndc": "62332-071-10", "marketing_start_date": "20250331"}, {"sample": false, "description": "25 VIAL in 1 CARTON (62332-071-25)  / 10 mL in 1 VIAL", "package_ndc": "62332-071-25", "marketing_start_date": "20250331"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "62332-071_db0264f6-5825-49a1-bb86-746ece155660", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62332-071", "generic_name": "pantoprazole sodium injection", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA219230", "marketing_category": "ANDA", "marketing_start_date": "20250331", "listing_expiration_date": "20261231"}