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These highlights do not include all the information needed to use NOXAFIL safely and effectively. See full prescribing information for NOXAFIL. NOXAFIL® (posaconazole) injection, for intravenous use NOXAFIL® (posaconazole) delayed-release tablets, for oral useNOXAFIL® (posaconazole) oral suspensionNOXAFIL® PowderMix (posaconazole) for delayed-release oral suspensionInitial U.S. Approval: 2006
Medication labelWhy this: Advisory · dailymed-prescription
Noxafil® injection and Noxafil delayed-release tablets are indicated for the treatment of invasive aspergillosis in adults and pediatric patients 13 years of age and older. Noxafil is indicated for the prophylaxis of invasive Aspergillus and Candida infections in patients who are at high risk of developing these infections due to being severely immunocompromised, such as hematopoietic stem cell transplant (HSCT) recipients with graft-versus-host disease (GVHD) or those with hematologic malignancies with prolonged neutropenia from chemotherapy [see Clinical Studies (14.1)] as follows: Noxafil injection: adults and pediatric patients 2 years of age and older Noxafil delayed-release tablets: adults and pediatric patients 2 years of age and older who weigh greater than 40 kg Noxafil oral suspension: adults and pediatric patients 13 years of age and older Noxafil PowderMix for delayed-release oral suspension: pediatric patients 2 years of age and older who weigh 40 kg or less Noxafil oral suspension is indicated for the treatment of oropharyngeal candidiasis, including oropharyngeal candidiasis refractory to itraconazole and/or fluconazole in adults and pediatric patients 13 years of age and older.
- generic_name
- posaconazole
- product_names
- posaconazole
- ndc
- 0085-1328, 0085-1328-01, 0085-4324, 0085-4324-02, 0085-4331, 0085-4331-01, 0085-2224, 0085-2224-01, 0085-2224-02
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en