# DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE

NDC: 11534-196
Generic name: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Labeler / Manufacturer: SUNRISE PHARMACEUTICAL, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180704

FDA application: ANDA209799

## Active ingredients

- AMPHETAMINE ASPARTATE MONOHYDRATE: 7.5 mg/1
- AMPHETAMINE SULFATE: 7.5 mg/1
- DEXTROAMPHETAMINE SACCHARATE: 7.5 mg/1
- DEXTROAMPHETAMINE SULFATE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11534-196"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11534-196
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ac102599-3a5b-4154-899e-6ff262be7ff7