Package 71839-122-01

{"route": ["INTRAVENOUS"], "spl_id": "bad4fab9-654b-423c-87dc-25ff7a9f29d9", "openfda": {"upc": ["0371839122011"], "unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["52d5bc28-66df-43aa-bb1a-8ac4a2a7f693"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (71839-122-01)  / 10 mL in 1 VIAL", "package_ndc": "71839-122-01", "marketing_start_date": "20220525"}, {"sample": false, "description": "10 CARTON in 1 PACKAGE (71839-122-10)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL", "package_ndc": "71839-122-10", "marketing_start_date": "20220525"}, {"sample": false, "description": "25 CARTON in 1 PACKAGE (71839-122-25)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL", "package_ndc": "71839-122-25", "marketing_start_date": "20220525"}], "brand_name": "Pantoprazole sodium", "product_id": "71839-122_bad4fab9-654b-423c-87dc-25ff7a9f29d9", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71839-122", "generic_name": "Pantoprazole sodium", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA216171", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}