# Probenecid

NDC: 16571-831
Generic name: Probenecid
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20231120

FDA application: ANDA217020

## Active ingredients

- PROBENECID: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-831"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-831
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2375d90-4132-4fb6-aee7-c4f9d11e98d5