Application Nr Approved Date Route Status External Links
NDA022569 None Nasal None Google , Wikipedia , PubMed , DailyMed , Raw OpenFDA , ECHA , ToxNet , JECFA , FAO , 21 CFR

Indications and Purposes

Indications And Usage Lazanda Is Indicated For The Management Of Breakthrough Pain In Cancer Patients 18 Years Of Age And Older Who Are Already Receiving And Who Are Tolerant To Around-The-Clock Opioid Therapy For Their Underlying Persistent Cancer Pain. Patients Considered Opioid Tolerant Are Those Who Are Taking, For One Week Or Longer, Around-The-Clock Medicine Consisting Of At Least: 60 Mg Of Oral Morphine Per Day, 25 Mcg Of Transdermal Fentanyl Per Hour, 30 Mg Oral Oxycodone Per Day, 8 Mg Oral Hydromorphone Per Day, Or At Least 25 Mg Oral Oxymorphone Per Day, Or At Least 60mg Oral Hydrocodone Per Day, Or An Equianalgesic Dose Of Another Opioid For A Week Or Longer. Patients Must Remain On Around-The-Clock Opioids When Taking Lazanda. Limitations Of Use: Not For Use In Opioid Non-Tolerant Patients. Not For Use In The Management Of Acute Or Postoperative Pain, Including Headache/migraine, Dental Pain, Or In The Emergency Department [See Contraindications ( 4 )]. As A Part Of The Tirf Rems Access Program, Lazanda May Be Dispensed Only To Outpatients Enrolled In The Program. [See Warnings And Precautions ( 5.7 )] . For Inpatient Administration Of Lazanda (E.g. Hospitals, Hospices, And Long-Term Care Facilities That Prescribe For Inpatient Use), Patient Enrollment Is Not Required.

All Formulated Excipients (0 Total)

None

Active Ingredients ( 1 Total)

Name Structure ZINC ID(s)
1. Fentanyl Citrate FENTANYL CITRATE ZINC2522669

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