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"68382-671-05" National Drug Code (NDC)

Amiloride Hydrochloride 500 TABLET in 1 BOTTLE (68382-671-05)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-671-05
Package Description500 TABLET in 1 BOTTLE (68382-671-05)
Product NDC68382-671
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmiloride Hydrochloride
Non-Proprietary NameAmiloride Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20150914
Marketing Category NameANDA
Application NumberANDA204180
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameAMILORIDE HYDROCHLORIDE
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/68382-671-05





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