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

NDC: 64850-504
Generic name: Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Labeler / Manufacturer: Elite Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20221229

FDA application: ANDA211352

## Active ingredients

- AMPHETAMINE ASPARTATE MONOHYDRATE: 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:"64850-504"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64850-504
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e677690f-790f-4626-ad78-097cdb6ea540