# Phentermine hydrochloride

NDC: 11534-159
Generic name: phentermine hydrochloride
Labeler / Manufacturer: SUNRISE PHARMACEUTICAL, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170124

FDA application: ANDA205017

## Active ingredients

- PHENTERMINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11534-159"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11534-159
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43024f64-2d77-49a9-80fd-ad07a86c69a3