Package 0008-4001-25

{"route": ["INTRAVENOUS"], "spl_id": "d36cd2fb-517f-44e5-8438-53e563775f86", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669", "885257"], "spl_set_id": ["f39b3e7d-39d2-4c8a-9974-4ab885241880"], "manufacturer_name": ["Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 PACKAGE (0008-4001-10)  / 1 VIAL in 1 CARTON (0008-4001-01)  / 10 mL in 1 VIAL", "package_ndc": "0008-4001-10", "marketing_start_date": "20130501"}, {"sample": false, "description": "25 CARTON in 1 PACKAGE (0008-4001-25)  / 1 VIAL in 1 CARTON (0008-4001-01)  / 10 mL in 1 VIAL", "package_ndc": "0008-4001-25", "marketing_start_date": "20130501"}], "brand_name": "Protonix I.V.", "product_id": "0008-4001_d36cd2fb-517f-44e5-8438-53e563775f86", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0008-4001", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Protonix", "brand_name_suffix": "I.V.", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "NDA020988", "marketing_category": "NDA", "marketing_start_date": "20130501", "listing_expiration_date": "20261231"}