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"63629-2114-1" National Drug Code (NDC)

Amiloride Hydrochloride 1000 TABLET in 1 BOTTLE (63629-2114-1)
(Bryant Ranch Prepack)

NDC Code63629-2114-1
Package Description1000 TABLET in 1 BOTTLE (63629-2114-1)
Product NDC63629-2114
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmiloride Hydrochloride
Non-Proprietary NameAmiloride Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date19860122
Marketing Category NameANDA
Application NumberANDA070346
ManufacturerBryant Ranch Prepack
Substance NameAMILORIDE HYDROCHLORIDE ANHYDROUS
Strength5
Strength Unitmg/1
Pharmacy ClassesDecreased Renal K+ Excretion [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63629-2114-1





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