United States · FDA National Drug Code directory

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate

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
42858-721_124f93d9-2c76-480c-82f5-43a6d9fdb87b
Product NDC
42858-721
Form
TABLET
Composition / generic term
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate
Labeler
Rhodes Pharmaceuticals LLC
Marketing category
ANDA
Marketing start / end (source format)
20210909
Source listing expiry
20271231

Source-listed ingredients

  • DEXTROAMPHETAMINE SACCHARATE — 1.25 mg/1
  • AMPHETAMINE ASPARTATE MONOHYDRATE — 1.25 mg/1
  • DEXTROAMPHETAMINE SULFATE — 1.25 mg/1
  • AMPHETAMINE SULFATE — 1.25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (42858-721-01) · 42858-721-01

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 →