"53002-6441-1" National Drug Code (NDC)

Montelukast 30 TABLET, FILM COATED in 1 BOTTLE (53002-6441-1)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-6441-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (53002-6441-1)
Product NDC53002-6441
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140910
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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