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

NDC: 0527-0792
Generic name: Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amphetamine Sulfate and Amphetamine Aspartate
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20211126

FDA application: ANDA214403

## 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:"0527-0792"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-0792