# Zenzedi

NDC: 24338-855
Generic name: Dextroamphetamine Sulfate
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140501

FDA application: ANDA090533

## Active ingredients

- DEXTROAMPHETAMINE SULFATE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24338-855"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24338-855
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d6394df5-f2c9-47eb-b57e-f3e9cfd94f84