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"68071-1652-9" National Drug Code (NDC)
Montelukast 90 TABLET, FILM COATED in 1 BOTTLE (68071-1652-9)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-1652-9
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (68071-1652-9)
Product NDC
68071-1652
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Montelukast
Non-Proprietary Name
Montelukast
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20141201
Marketing Category Name
ANDA
Application Number
ANDA202859
Manufacturer
NuCare 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/68071-1652-9