NDC 68180-803 – Rufinamide

Rufinamide 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68180-803

Product details

Brand name
Rufinamide
Generic name
Rufinamide
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204964
Marketed since
November 28, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Rufinamide →

Package NDC codes (1)

Package NDCDescriptionSince
68180-803-16120 TABLET, FILM COATED in 1 BOTTLE (68180-803-16)Nov 28, 2022

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