United States · FDA National Drug Code directory

DEXTROAMPHETAMINE 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
11534-189_b4a1b595-c7dd-47f8-8512-a05bea0b5425
Product NDC
11534-189
Form
TABLET
Composition / generic term
dextroamphetamine sulfate
Labeler
SUNRISE PHARMACEUTICAL, INC.
Marketing category
ANDA
Marketing start / end (source format)
20180704
Source listing expiry
20271231

Source-listed ingredients

  • DEXTROAMPHETAMINE SULFATE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (11534-189-01) · 11534-189-01
  • 1000 TABLET in 1 BOTTLE (11534-189-03) · 11534-189-03

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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DEXTROAMPHETAMINE SULFATE — United States | Molindra Medicines