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"57721-671-05" National Drug Code (NDC)
Amiloride Hydrochloride 500 TABLET in 1 BOTTLE (57721-671-05)
(WINDLAS BIOTECH LIMITED)
NDC Code
57721-671-05
Package Description
500 TABLET in 1 BOTTLE (57721-671-05)
Product NDC
57721-671
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amiloride Hydrochloride
Non-Proprietary Name
Amiloride Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20211201
Marketing Category Name
ANDA
Application Number
ANDA204180
Manufacturer
WINDLAS BIOTECH LIMITED
Substance Name
AMILORIDE HYDROCHLORIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57721-671-05