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"47335-175-88" National Drug Code (NDC)

Levocetirizine Dihydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (47335-175-88)
(Sun Pharma Global FZE)

NDC Code47335-175-88
Package Description100 TABLET, FILM COATED in 1 BOTTLE (47335-175-88)
Product NDC47335-175
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLevocetirizine Dihydrochloride
Non-Proprietary NameLevocetirizine Dihydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130205
End Marketing Date20171031
Marketing Category NameANDA
Application NumberANDA090362
ManufacturerSun Pharma Global FZE
Substance NameLEVOCETIRIZINE DIHYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-175-88





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