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"0173-0922-45" National Drug Code (NDC)

Blujepa 20 TABLET, FILM COATED in 1 BOTTLE (0173-0922-45)
(GlaxoSmithKline LLC)

NDC Code0173-0922-45
Package Description20 TABLET, FILM COATED in 1 BOTTLE (0173-0922-45)
Product NDC0173-0922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBlujepa
Non-Proprietary NameGepotidacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250325
Marketing Category NameNDA
Application NumberNDA218230
ManufacturerGlaxoSmithKline LLC
Substance NameGEPOTIDACIN MESYLATE
Strength750
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0173-0922-45





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