ELIGARD
Leuprolide Acetate · KIT · TOLMAR Inc.
No Recall History
Plain English
ELIGARD is a kit containing leuprolide acetate, taken subcutaneous. Manufactured by TOLMAR Inc..
Key Facts
- Brand Name
- ELIGARD
- Generic Name
- Leuprolide Acetate
- NDC Code (Product)
62935-223- Manufacturer
- TOLMAR Inc.
- Dosage Form
- KIT
- Route
- SUBCUTANEOUS
- Marketing Status
- Application #
- NDA021379
- Marketing Start
- 08/26/2002
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
intercepted product preparation error8,869 reports
syringe issue7,730 reports
hot flush6,264 reports
death6,260 reports
device leakage5,988 reports
wrong technique in product usage process5,213 reports
injection site pain4,198 reports
fatigue3,463 reports
prostatic specific antigen increased1,924 reports
intentional product use issue1,647 reports
Frequently Asked Questions
What is ELIGARD used for?
ELIGARD contains Leuprolide Acetate. It is a kit taken subcutaneous. Consult your doctor for specific uses.
Is ELIGARD a controlled substance?
ELIGARD is not classified as a controlled substance by the DEA.
What is the generic name for ELIGARD?
The generic name for ELIGARD is Leuprolide Acetate. There are 11 other brand versions of Leuprolide Acetate.
What is the NDC code for ELIGARD ?
The NDC (National Drug Code) for ELIGARD is 62935-223, listed by TOLMAR Inc..