"49884-117-05" National Drug Code (NDC)

Amiloride Hydrochloride 500 TABLET in 1 BOTTLE (49884-117-05)
(Par Pharmaceutical Inc.)

NDC Code49884-117-05
Package Description500 TABLET in 1 BOTTLE (49884-117-05)
Product NDC49884-117
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmiloride Hydrochloride
Non-Proprietary NameAmiloride Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date19860122
Marketing Category NameANDA
Application NumberANDA070346
ManufacturerPar Pharmaceutical Inc.
Substance NameAMILORIDE HYDROCHLORIDE ANHYDROUS
Strength5
Strength Unitmg/1
Pharmacy ClassesDecreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC]

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