Drugplain

Blujepa 750 mg/1

gepotidacin · TABLET, FILM COATED · GlaxoSmithKline LLC

No Recall History
Plain English

Blujepa is a tablet, film coated containing gepotidacin at 750 mg/1, taken oral. Manufactured by GlaxoSmithKline LLC.

Key Facts

Brand Name
Blujepa
Generic Name
gepotidacin
NDC Code (Product)
0173-0922
Manufacturer
GlaxoSmithKline LLC
Strength
750 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA218230
Marketing Start
03/25/2025

Recall History

No Recall History

Frequently Asked Questions

What is Blujepa used for?

Blujepa contains gepotidacin. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Blujepa a controlled substance?

Blujepa is not classified as a controlled substance by the DEA.

What is the generic name for Blujepa?

The generic name for Blujepa is gepotidacin. There are no other listed brand versions of gepotidacin.

What is the NDC code for Blujepa 750 mg/1?

The NDC (National Drug Code) for Blujepa 750 mg/1 is 0173-0922, listed by GlaxoSmithKline LLC.

Product NDC

0173-0922

Package NDC

0173-0922-38

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)