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
- 16714-950_74be2e0b-bbf0-448a-b035-316834bb4118
- Product NDC
- 16714-950
- Form
- TABLET
- Composition / generic term
- Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
- Labeler
- NorthStar RxLLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190320
- Source listing expiry
- 20261231
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 (16714-950-01) · 16714-950-01
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 →