NDC 49502-476 – Pretomanid

Pretomanid 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC49502-476

Product details

Brand name
Pretomanid
Generic name
Pretomanid
Labeler
Viatris Specialty LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA212862
Marketed since
November 7, 2019
Listing expires
December 31, 2026
Pharmacologic class
Antimycobacterial

Active ingredients

Uses, dosage, side effects and warnings for Pretomanid →

Package NDC codes (1)

Package NDCDescriptionSince
49502-476-261 BOTTLE in 1 CARTON (49502-476-26) / 26 TABLET in 1 BOTTLENov 7, 2019