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"68151-0162-0" National Drug Code (NDC)
Amiloride Hydrochloride 1 TABLET in 1 PACKAGE (68151-0162-0)
(Carilion Materials Management)
NDC Code
68151-0162-0
Package Description
1 TABLET in 1 PACKAGE (68151-0162-0)
Product NDC
68151-0162
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amiloride Hydrochloride
Non-Proprietary Name
Amiloride Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
19860122
Marketing Category Name
ANDA
Application Number
ANDA070346
Manufacturer
Carilion Materials Management
Substance Name
AMILORIDE HYDROCHLORIDE ANHYDROUS
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/68151-0162-0