"57721-671-01" National Drug Code (NDC)

Amiloride Hydrochloride 100 TABLET in 1 BOTTLE (57721-671-01)
(WINDLAS BIOTECH LIMITED)

NDC Code57721-671-01
Package Description100 TABLET in 1 BOTTLE (57721-671-01)
Product NDC57721-671
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmiloride Hydrochloride
Non-Proprietary NameAmiloride Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20211201
Marketing Category NameANDA
Application NumberANDA204180
ManufacturerWINDLAS BIOTECH LIMITED
Substance NameAMILORIDE HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesDecreased Renal K+ Excretion [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC]

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