Package 0781-3531-91

{"route": ["INTRAVENOUS"], "spl_id": "374cacf2-c5ef-4958-e063-6294a90a5b3c", "openfda": {"nui": ["N0000175085", "N0000175592"], "upc": ["0307813531913"], "unii": ["P88XT4IS4D"], "rxcui": ["583214"], "spl_set_id": ["15ca4829-8fee-45f9-b4bc-b31c15732cd6"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3531-91)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0781-3531-91", "marketing_start_date": "20241009"}], "brand_name": "Paclitaxel", "product_id": "0781-3531_374cacf2-c5ef-4958-e063-6294a90a5b3c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "0781-3531", "generic_name": "Paclitaxel", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paclitaxel", "active_ingredients": [{"name": "PACLITAXEL", "strength": "100 mg/20mL"}], "application_number": "ANDA212700", "marketing_category": "ANDA", "marketing_start_date": "20241008", "listing_expiration_date": "20261231"}