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"31722-726-31" National Drug Code (NDC)

Montelukast 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-726-31)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-726-31
Package Description10 TABLET, FILM COATED in 1 BLISTER PACK (31722-726-31)
Product NDC31722-726
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140910
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerCamber Pharmaceuticals, Inc.
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/31722-726-31





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