FDA NDC Directory · JSON-LD · Markdown

DIURIL

NDC 65649-311 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Generic nameCHLOROTHIAZIDE
Labeler / ManufacturerSalix Pharmaceuticals, Inc
Marketing categoryNew Drug Application (innovator) · App NDA011870
Dosage form / routeSUSPENSION · ORAL
Active ingredientsCHLOROTHIAZIDE (250 mg/5mL)
Marketing started19620215
Marketing ended20280131
Package count1

External sources

Source: openFDA. Public-domain (CC0).