# AMPHETAMINE SULFATE

NDC: 72162-1369
Generic name: amphetamine sulfate
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200402

FDA application: ANDA211861

## Active ingredients

- AMPHETAMINE SULFATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1369"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1369
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7f16dd18-bf30-41ef-8981-932da5df0951