# Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate

NDC: 55466-131
Generic name: Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Labeler / Manufacturer: Neolpharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250205

FDA application: ANDA210754

## Active ingredients

- AMPHETAMINE ASPARTATE: 3.75 mg/1
- AMPHETAMINE SULFATE: 3.75 mg/1
- DEXTROAMPHETAMINE SACCHARATE: 3.75 mg/1
- DEXTROAMPHETAMINE SULFATE: 3.75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55466-131"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55466-131
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c922de13-7ae0-a09c-e053-2995a90a4411