Package 25021-751-10

{"route": ["INTRAVENOUS"], "spl_id": "2b04a735-571c-4668-bc78-ac3a611d575c", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["c39be14b-e881-4586-b77e-4747db494954"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-751-10)  / 10 mL in 1 VIAL", "package_ndc": "25021-751-10", "marketing_start_date": "20220715"}, {"sample": false, "description": "25 VIAL in 1 CARTON (25021-751-11)  / 10 mL in 1 VIAL", "package_ndc": "25021-751-11", "marketing_start_date": "20220715"}], "brand_name": "Pantoprazole Sodium", "product_id": "25021-751_2b04a735-571c-4668-bc78-ac3a611d575c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "25021-751", "generic_name": "Pantoprazole Sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA204400", "marketing_category": "ANDA", "marketing_start_date": "20220715", "listing_expiration_date": "20261231"}