NDC 0173-0922 – Blujepa

Gepotidacin Mesylate 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0173-0922

Product details

Brand name
Blujepa
Generic name
gepotidacin
Labeler
GlaxoSmithKline LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA218230
Marketed since
March 25, 2025
Listing expires
December 31, 2027
Pharmacologic class
Triazaacenaphthylene Bacterial Type II Topoisomerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Blujepa →

Package NDC codes (2)

Package NDCDescriptionSince
0173-0922-388 TABLET, FILM COATED in 1 BOTTLE (0173-0922-38)Dec 11, 2025
0173-0922-4520 TABLET, FILM COATED in 1 BOTTLE (0173-0922-45)Mar 25, 2025