# Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate

NDC: 57664-641
Generic name: Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20030909

FDA application: ANDA040480

## Active ingredients

- AMPHETAMINE ASPARTATE: 1.25 mg/1
- AMPHETAMINE SULFATE: 1.25 mg/1
- DEXTROAMPHETAMINE SACCHARATE: 1.25 mg/1
- DEXTROAMPHETAMINE SULFATE: 1.25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-641"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-641
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9af67219-9b37-45d0-ac52-647cbfacd296