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"47335-175-83" National Drug Code (NDC)
Levocetirizine Dihydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (47335-175-83)
(Sun Pharma Global FZE)
NDC Code
47335-175-83
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (47335-175-83)
Product NDC
47335-175
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Levocetirizine Dihydrochloride
Non-Proprietary Name
Levocetirizine Dihydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20130205
End Marketing Date
20171031
Marketing Category Name
ANDA
Application Number
ANDA090362
Manufacturer
Sun Pharma Global FZE
Substance Name
LEVOCETIRIZINE DIHYDROCHLORIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-175-83