# Benzphetamine Hydrochloride

NDC: 42806-081
Generic name: Benzphetamine Hydrochloride
Labeler / Manufacturer: Epic Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20151216

FDA application: ANDA090346

## Active ingredients

- BENZPHETAMINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42806-081"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-081
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6d9b369-4b64-4d3f-844d-5d60dd257c55