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"0173-0835-13" National Drug Code (NDC)

Avandia 30 TABLET, FILM COATED in 1 BOTTLE (0173-0835-13)
(GlaxoSmithKline LLC)

NDC Code0173-0835-13
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0173-0835-13)
Product NDC0173-0835
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAvandia
Non-Proprietary NameRosiglitazone Maleate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110525
End Marketing Date20150829
Marketing Category NameNDA
Application NumberNDA021071
ManufacturerGlaxoSmithKline LLC
Substance NameROSIGLITAZONE MALEATE
Strength4
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor gamma Agonist [EPC],Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0173-0835-13





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