FDA NDC Directory · JSON-LD · Markdown

Azulfidine EN-tabs

NDC 0013-0102 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic nameSulfasalazine
Labeler / ManufacturerPfizer Laboratories Div Pfizer Inc
Marketing categoryNew Drug Application (innovator) · App NDA007073
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsSULFASALAZINE (500 mg/1)
Marketing started19500620
Package count2

External sources

Source: openFDA. Public-domain (CC0).