"0173-0922-38" National Drug Code (NDC)

NDC Code	0173-0922-38
Package Description	8 TABLET, FILM COATED in 1 BOTTLE (0173-0922-38)
Product NDC	0173-0922
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Blujepa
Non-Proprietary Name	Gepotidacin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20250325
Marketing Category Name	NDA
Application Number	NDA218230
Manufacturer	GlaxoSmithKline LLC
Substance Name	GEPOTIDACIN MESYLATE
Strength	750
Strength Unit	mg/1
Pharmacy Classes	Cholinesterase Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA], Topoisomerase 2 Inhibitors [MoA], Topoisomerase 4 Inhibitors [MoA], Triazaacenaphthylene Bacterial Type II Topoisomerase Inhibitor [EPC]