# Phentermine hydrochloride

NDC: 52605-022
Generic name: Phentermine hydrochloride
Labeler / Manufacturer: POLYGEN PHARMACEUTICALS INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20161118

FDA application: ANDA206342

## 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:"52605-022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52605-022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e47dc31f-9548-403e-940f-a5380f938aed