{"effective_time":"20230728","id":"41b76e97-b780-4fc8-b073-13bf155ad8a5","openfda":{"application_number":["ANDA208980"],"brand_name":["PLERIXAFOR"],"generic_name":["PLERIXAFOR"],"is_original_packager":[true],"manufacturer_name":["Zydus Lifesciences Limited"],"nui":["N0000178326","N0000178324"],"package_ndc":["70771-1776-1"],"pharm_class_epc":["Hematopoietic Stem Cell Mobilizer [EPC]"],"pharm_class_pe":["Increased Hematopoietic Stem Cell Mobilization [PE]"],"product_ndc":["70771-1776"],"product_type":["HUMAN PRESCRIPTION DRUG"],"route":["SUBCUTANEOUS"],"rxcui":["828700"],"spl_id":["41b76e97-b780-4fc8-b073-13bf155ad8a5"],"spl_set_id":["43df348a-d7f2-4f14-8131-c916679a98eb"],"substance_name":["PLERIXAFOR"],"unii":["S915P5499N"]},"package_label_principal_display_panel":["PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1776-1 Plerixafor Injection – 1.2 mL vial label 24 mg/1.2 mL (20 mg/mL) For subcutaneous injection only For single-dose only Rx only NDC 70771-1776-1 Carton contains one vial of Plerixafor Injection 24 mg/1.2 mL (20 mg/mL) For subcutaneous injection only See package insert for dosage and administration For single-dose only Rx only vial label carton label"],"set_id":"43df348a-d7f2-4f14-8131-c916679a98eb","spl_product_data_elements":["PLERIXAFOR plerixafor PLERIXAFOR PLERIXAFOR HYDROCHLORIC ACID SODIUM CHLORIDE SODIUM HYDROXIDE WATER"],"spl_unclassified_section":[""],"version":"1"}