DALFAMPRIDINE 10 mg/1
DALFAMPRIDINE · TABLET, FILM COATED, EXTENDED RELEASE · Aurobindo Pharma Limited
No Recall History
Plain English
DALFAMPRIDINE is a tablet, film coated, extended release containing dalfampridine at 10 mg/1, taken oral. Manufactured by Aurobindo Pharma Limited.
Key Facts
- Brand Name
- DALFAMPRIDINE
- Generic Name
- DALFAMPRIDINE
- NDC Code (Product)
65862-863- Manufacturer
- Aurobindo Pharma Limited
- Strength
- 10 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA206811
- Drug Class
- Potassium Channel Blocker [EPC]
- Marketing Start
- 06/25/2018
Recall History
No Recall HistoryFrequently Asked Questions
What is DALFAMPRIDINE used for?
DALFAMPRIDINE contains DALFAMPRIDINE. It is a tablet, film coated, 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 9 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 65862-863, listed by Aurobindo Pharma Limited.