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Pretomanid

NDC 49502-476 · Viatris Specialty LLC

Generic namePretomanid
Dosage formTABLET
RouteORAL
Active ingredient(s)PRETOMANID
Strength200 mg/1
Pharmacologic classAntimycobacterial [EPC], Organic Anion Transporter 3 Inhibitors [MoA]
Marketing categoryNDA

Packages

49502-476-26 — 1 BOTTLE in 1 CARTON (49502-476-26) / 26 TABLET in 1 BOTTLE

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels