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"51672-2097-1" National Drug Code (NDC)
Cetirizine Hydrochloride 1 BOTTLE in 1 CARTON (51672-2097-1) > 100 TABLET in 1 BOTTLE
(Taro Pharmaceuticals U.S.A., Inc.)
NDC Code
51672-2097-1
Package Description
1 BOTTLE in 1 CARTON (51672-2097-1) > 100 TABLET in 1 BOTTLE
Product NDC
51672-2097
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20090722
Marketing Category Name
ANDA
Application Number
ANDA078072
Manufacturer
Taro Pharmaceuticals U.S.A., 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/51672-2097-1