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
16714-803_0e86a41d-6f4d-238f-e063-6294a90a8ab2
Product NDC
16714-803
Form
TABLET
Composition / generic term
Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate
Labeler
Northstar Rx LLC
Marketing category
ANDA
Marketing start / end (source format)
20030909
Source listing expiry
20261231

Source-listed ingredients

  • DEXTROAMPHETAMINE SACCHARATE — 1.875 mg/1
  • AMPHETAMINE ASPARTATE — 1.875 mg/1
  • DEXTROAMPHETAMINE SULFATE — 1.875 mg/1
  • AMPHETAMINE SULFATE — 1.875 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE, PLASTIC (16714-803-01) · 16714-803-01

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 →
Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate — United States | Molindra Medicines