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"16714-832-02" National Drug Code (NDC)

Bumetanide 500 TABLET in 1 BOTTLE (16714-832-02)
(Northstar Rx LLC)

NDC Code16714-832-02
Package Description500 TABLET in 1 BOTTLE (16714-832-02)
Product NDC16714-832
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBumetanide
Non-Proprietary NameBumetanide
Dosage FormTABLET
UsageORAL
Start Marketing Date20180625
Marketing Category NameANDA
Application NumberANDA202900
ManufacturerNorthstar Rx LLC
Substance NameBUMETANIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-832-02





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