# Amphetamine Sulfate

NDC: 70010-041
Generic name: Amphetamine Sulfate
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190815

FDA application: ANDA212619

## 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:"70010-041"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-041
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=26dbad66-13c4-4906-88b3-ab7ee191466c