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"68001-361-03" National Drug Code (NDC)

Montelukast 500 TABLET in 1 BOTTLE (68001-361-03)
(BluePoint Laboratories)

NDC Code68001-361-03
Package Description500 TABLET in 1 BOTTLE (68001-361-03)
Product NDC68001-361
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET
UsageORAL
Start Marketing Date20180629
Marketing Category NameANDA
Application NumberANDA203366
ManufacturerBluePoint Laboratories
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/68001-361-03





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