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

NDC: 57664-950
Generic name: Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240201

FDA application: ANDA215997

## Active ingredients

- AMPHETAMINE ASPARTATE MONOHYDRATE: 3.125 mg/1
- AMPHETAMINE SULFATE: 3.125 mg/1
- DEXTROAMPHETAMINE SACCHARATE: 3.125 mg/1
- DEXTROAMPHETAMINE SULFATE: 3.125 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-950"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-950
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30e515c3-a18f-499a-87c4-be8d64cfdbc6