FDA NDC Directory · JSON-LD · Markdown

Probenecid

NDC 10135-541 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMarlex Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA080966
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPROBENECID (500 mg/1)
Marketing started19760729
Package count2

External sources

Source: openFDA. Public-domain (CC0).