United States · FDA National Drug Code directory

Lisdexamfetamine dimesylate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
72205-134_a79cb70c-0bfa-4d68-9a21-a5ef4bc3c811
Product NDC
72205-134
Form
TABLET, CHEWABLE
Composition / generic term
Lisdexamfetamine dimesylate
Labeler
Novadoz Pharmaceuticals LLC
Marketing category
ANDA
Marketing start / end (source format)
20240202
Source listing expiry
20261231

Source-listed ingredients

  • LISDEXAMFETAMINE DIMESYLATE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, CHEWABLE in 1 BOTTLE (72205-134-91) · 72205-134-91

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →