"42291-122-90" National Drug Code (NDC)

Amiloride Hydrochloride 90 TABLET in 1 BOTTLE (42291-122-90)
(AvKARE, Inc.)

NDC Code42291-122-90
Package Description90 TABLET in 1 BOTTLE (42291-122-90)
Product NDC42291-122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmiloride Hydrochloride
Non-Proprietary NameAmiloride Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20120328
Marketing Category NameANDA
Application NumberANDA079133
ManufacturerAvKARE, Inc.
Substance NameAMILORIDE HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesDecreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC]

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