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"16571-678-10" National Drug Code (NDC)

Bumetanide 1000 TABLET in 1 BOTTLE (16571-678-10)
(Rising Pharma Holdings, Inc)

NDC Code16571-678-10
Package Description1000 TABLET in 1 BOTTLE (16571-678-10)
Product NDC16571-678
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBumetanide
Non-Proprietary NameBumetanide
Dosage FormTABLET
UsageORAL
Start Marketing Date20240603
Marketing Category NameANDA
Application NumberANDA212019
ManufacturerRising Pharma Holdings, Inc
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/16571-678-10





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