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"72865-175-10" National Drug Code (NDC)
Montelukast 1000 TABLET, FILM COATED in 1 BOTTLE (72865-175-10)
(XLCare Pharmaceuticals Inc.)
NDC Code
72865-175-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (72865-175-10)
Product NDC
72865-175
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Montelukast
Non-Proprietary Name
Montelukast
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210211
Marketing Category Name
ANDA
Application Number
ANDA202843
Manufacturer
XLCare Pharmaceuticals Inc.
Substance Name
MONTELUKAST SODIUM
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72865-175-10