FDA NDC Directory · JSON-LD · Markdown

Probenecid

NDC 70518-4649 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA217020
Dosage form / routeTABLET · ORAL
Active ingredientsPROBENECID (500 mg/1)
Marketing started20260428
Package count1

External sources

Source: openFDA. Public-domain (CC0).