# Cephalexin

NDC: 71205-672
Generic name: Cephalexin
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20110119

FDA application: ANDA090836

## Active ingredients

- CEPHALEXIN: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-672"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-672
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7059a0b2-dd57-4fc1-ac3d-6aead35a4b08