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"51079-223-20" National Drug Code (NDC)
Montelukast Sodium 100 BLISTER PACK in 1 CARTON (51079-223-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-223-01)
(Mylan Institutional Inc.)
NDC Code
51079-223-20
Package Description
100 BLISTER PACK in 1 CARTON (51079-223-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-223-01)
Product NDC
51079-223
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Montelukast Sodium
Non-Proprietary Name
Montelukast Sodium
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20120828
End Marketing Date
20190930
Marketing Category Name
ANDA
Application Number
ANDA079103
Manufacturer
Mylan Institutional 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/51079-223-20