# Phentermine Hydrochloride

NDC: 10702-025
Generic name: Phentermine Hydrochloride
Labeler / Manufacturer: KVK-TECH, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20120815

FDA application: ANDA040876

## 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:"10702-025"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-025
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b44d104-a7d0-4366-9d42-63f784f3cb22