"70756-080-51" National Drug Code (NDC)

Bumetanide 500 TABLET in 1 BOTTLE (70756-080-51)
(Lifestar Pharma LLC)

NDC Code70756-080-51
Package Description500 TABLET in 1 BOTTLE (70756-080-51)
Product NDC70756-080
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBumetanide
Non-Proprietary NameBumetanide
Dosage FormTABLET
UsageORAL
Start Marketing Date20250403
Marketing Category NameANDA
Application NumberANDA219291
ManufacturerLifestar Pharma LLC
Substance NameBUMETANIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]

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