FDA NDC Directory · JSON-LD · Markdown

Pretomanid

NDC 49502-476 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerViatris Specialty LLC
Marketing categoryNew Drug Application (innovator) · App NDA212862
Dosage form / routeTABLET · ORAL
Active ingredientsPRETOMANID (200 mg/1)
Marketing started20191107
Package count1

External sources

Source: openFDA. Public-domain (CC0).