# Benzphetamine Hydrochloride

NDC: 23155-952
Generic name: Benzphetamine Hydrochloride
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260619

FDA application: ANDA202061

## 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:"23155-952"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-952
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=152a123e-4886-4184-a47d-462ce102b8fa