# Adderall

NDC: 57844-105
Generic name: Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20141113

FDA application: ANDA040422

## Active ingredients

- AMPHETAMINE ASPARTATE MONOHYDRATE: 1.25 mg/1
- AMPHETAMINE SULFATE: 1.25 mg/1
- DEXTROAMPHETAMINE SACCHARATE: 1.25 mg/1
- DEXTROAMPHETAMINE SULFATE: 1.25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57844-105"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57844-105
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f22635fe-821d-4cde-aa12-419f8b53db81