NDC 67919-041 – Sivextro

Tedizolid Phosphate 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC67919-041

Product details

Brand name
Sivextro
Generic name
Tedizolid phosphate
Labeler
Merck Sharp & Dohme LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA205435
Marketed since
June 20, 2014
Listing expires
December 31, 2027
Pharmacologic class
Oxazolidinone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Sivextro →

Package NDC codes (2)

Package NDCDescriptionSince
67919-041-0430 TABLET, FILM COATED in 1 BOTTLE (67919-041-04)Jun 20, 2014
67919-041-051 BLISTER PACK in 1 CARTON (67919-041-05) / 6 TABLET, FILM COATED in 1 BLISTER PACKJun 20, 2014

Other Sivextro products