FDA NDC Directory · JSON-LD · Markdown

Probenecid

NDC 16571-831 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217020
Dosage form / routeTABLET · ORAL
Active ingredientsPROBENECID (500 mg/1)
Marketing started20231120
Package count2

External sources

Source: openFDA. Public-domain (CC0).