Package 70095-024-02

{"route": ["INTRAVENOUS"], "spl_id": "b423abbc-01e1-4d07-9c89-a7398c898d2f", "openfda": {"upc": ["0370095024039"], "unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["eb3f58d4-0c69-4377-be45-c36099c98d33"], "manufacturer_name": ["Sun Pharmaceutical Industries Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 PACKAGE (70095-024-02)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)", "package_ndc": "70095-024-02", "marketing_start_date": "20230403"}, {"sample": false, "description": "25 CARTON in 1 PACKAGE (70095-024-03)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)", "package_ndc": "70095-024-03", "marketing_start_date": "20230403"}], "brand_name": "Pantoprazole sodium", "product_id": "70095-024_b423abbc-01e1-4d07-9c89-a7398c898d2f", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70095-024", "generic_name": "Pantoprazole sodium", "labeler_name": "Sun Pharmaceutical Industries Limited", "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": "20230403", "listing_expiration_date": "20261231"}