FDA NDC Directory · JSON-LD · Markdown

SULFATRIM

NDC 0121-0854 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Generic nameSulfamethoxazole and Trimethoprim
Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryNew Drug Application (innovator) · App NDA018615
Dosage form / routeSUSPENSION · ORAL
Active ingredientsSULFAMETHOXAZOLE (200 mg/5mL)
TRIMETHOPRIM (40 mg/5mL)
Marketing started19830703
Package count1

External sources

Source: openFDA. Public-domain (CC0).