NDC 65862-863 – Dalfampridine

Dalfampridine 10 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65862-863

Product details

Brand name
Dalfampridine
Generic name
Dalfampridine
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206811
Marketed since
June 25, 2018
Listing expires
December 31, 2026
Pharmacologic class
Potassium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Dalfampridine →

Package NDC codes (3)

Package NDCDescriptionSince
65862-863-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-863-01)Jun 25, 2018
65862-863-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-863-05)Jun 25, 2018
65862-863-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-863-60)Jun 25, 2018

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