United States · FDA National Drug Code directory
Dextroamphetamine Saccharate, Amphetamine Aspartate, 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
- 0527-0762_391d7c4a-47df-41ce-b1ba-3c4758adf87f
- Product NDC
- 0527-0762
- Form
- TABLET
- Composition / generic term
- Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
- Labeler
- Lannett Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220708
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXTROAMPHETAMINE SACCHARATE — 2.5 mg/1
- AMPHETAMINE ASPARTATE MONOHYDRATE — 2.5 mg/1
- DEXTROAMPHETAMINE SULFATE — 2.5 mg/1
- AMPHETAMINE SULFATE — 2.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0527-0762-37) · 0527-0762-37
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 →