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"51128-501-01" National Drug Code (NDC)

Montelukast 30 TABLET, FILM COATED in 1 BOTTLE (51128-501-01)
(Recipharm Pharmaservices Private Limited)

NDC Code51128-501-01
Package Description30 TABLET, FILM COATED in 1 BOTTLE (51128-501-01)
Product NDC51128-501
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20141201
Marketing Category NameANDA
Application NumberANDA202859
ManufacturerRecipharm Pharmaservices Private Limited
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51128-501-01





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