Dalfampridine 10 mg/1
Dalfampridine · TABLET, EXTENDED RELEASE · Sun Pharmaceutical Industries, Inc.
No Recall History
Plain English
Dalfampridine is a tablet, extended release containing dalfampridine at 10 mg/1, taken oral. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Dalfampridine
- Generic Name
- Dalfampridine
- NDC Code (Product)
62756-429- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 10 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA208292
- Drug Class
- Potassium Channel Blocker [EPC]
- Marketing Start
- 05/22/2019
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
fall1,052 reports
gait disturbance996 reports
drug ineffective826 reports
fatigue799 reports
covid-19581 reports
multiple sclerosis relapse568 reports
balance disorder548 reports
multiple sclerosis509 reports
asthenia433 reports
dizziness407 reports
Frequently Asked Questions
What is Dalfampridine used for?
Dalfampridine contains Dalfampridine. It is a tablet, extended release taken oral. Consult your doctor for specific uses.
Is Dalfampridine a controlled substance?
Dalfampridine is not classified as a controlled substance by the DEA.
What is the generic name for Dalfampridine?
The generic name for Dalfampridine is Dalfampridine. There are 5 other brand versions of Dalfampridine.
What is the NDC code for Dalfampridine 10 mg/1?
The NDC (National Drug Code) for Dalfampridine 10 mg/1 is 62756-429, listed by Sun Pharmaceutical Industries, Inc..