# Dextroamphetamine

NDC: 27808-085
Generic name: Dextroamphetamine
Labeler / Manufacturer: Cranbury Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20130531

FDA application: ANDA203644

## Active ingredients

- DEXTROAMPHETAMINE SULFATE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27808-085"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-085
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7658071e-ee2c-4d23-94ce-1906959ec036