United States · FDA National Drug Code directory

Amphetamine Extended-Release

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
62542-025_3f9283a3-e922-36ca-e063-6394a90a409d
Product NDC
62542-025
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
Amphetamine Extended-Release
Labeler
Neos Therapeutics, LP
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20250901
Source listing expiry
20261231

Source-listed ingredients

  • AMPHETAMINE — 15.7 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 BLISTER PACK in 1 CARTON (62542-025-30) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK · 62542-025-30

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.

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Amphetamine Extended-Release — United States | Molindra Medicines