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"82009-009-10" National Drug Code (NDC)

Montelukast 1000 TABLET, FILM COATED in 1 BOTTLE (82009-009-10)
(Quallent Pharmaceuticals Health LLC)

NDC Code82009-009-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (82009-009-10)
Product NDC82009-009
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220607
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerQuallent Pharmaceuticals Health LLC
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/82009-009-10





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