# Phentermine Hydrochloride

NDC: 63629-2477
Generic name: Phentermine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20110308
Marketing ended: 20280430
FDA application: ANDA200272

## 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:"63629-2477"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2477
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=328d6a39-34f4-4b74-a1bf-6ec6005b1322