"57721-671-30" National Drug Code (NDC)

Amiloride Hydrochloride 10 BLISTER PACK in 1 CARTON (57721-671-30) > 10 TABLET in 1 BLISTER PACK
(WINDLAS BIOTECH LIMITED)

NDC Code57721-671-30
Package Description10 BLISTER PACK in 1 CARTON (57721-671-30) > 10 TABLET in 1 BLISTER PACK
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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