"68382-527-10" National Drug Code (NDC)

Bumetanide 1000 TABLET in 1 BOTTLE (68382-527-10)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-527-10
Package Description1000 TABLET in 1 BOTTLE (68382-527-10)
Product NDC68382-527
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBumetanide
Non-Proprietary NameBumetanide
Dosage FormTABLET
UsageORAL
Start Marketing Date20180501
Marketing Category NameANDA
Application NumberANDA202900
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameBUMETANIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]

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