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"53002-1259-2" National Drug Code (NDC)
Cetirizine Hydrochloride 20 TABLET in 1 BOTTLE (53002-1259-2)
(RPK Pharmaceuticals, Inc.)
NDC Code
53002-1259-2
Package Description
20 TABLET in 1 BOTTLE (53002-1259-2)
Product NDC
53002-1259
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20091001
Marketing Category Name
ANDA
Application Number
ANDA077829
Manufacturer
RPK Pharmaceuticals, Inc.
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
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/53002-1259-2