NDC 42571-392 – Rufinamide

Rufinamide 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC42571-392

Product details

Brand name
Rufinamide
Generic name
Rufinamide
Labeler
Micro Labs Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216688
Marketed since
July 1, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Rufinamide →

Package NDC codes (1)

Package NDCDescriptionSince
42571-392-12120 TABLET in 1 BOTTLE (42571-392-12)Jul 1, 2023

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