www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"49884-117-10" National Drug Code (NDC)
Amiloride Hydrochloride 1000 TABLET in 1 BOTTLE (49884-117-10)
(Endo USA, Inc.)
NDC Code
49884-117-10
Package Description
1000 TABLET in 1 BOTTLE (49884-117-10)
Product NDC
49884-117
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
Endo USA, Inc.
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/49884-117-10