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"51672-2102-2" National Drug Code (NDC)
Childrens Cetirizine Hydrochloride 2 BOTTLE in 1 CARTON (51672-2102-2) / 120 mL in 1 BOTTLE
(Sun Pharmaceutical Industries, Inc.)
NDC Code
51672-2102-2
Package Description
2 BOTTLE in 1 CARTON (51672-2102-2) / 120 mL in 1 BOTTLE
Product NDC
51672-2102
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Childrens Cetirizine Hydrochloride
Proprietary Name Suffix
Sugar Free Grape
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
SOLUTION
Usage
ORAL
Start Marketing Date
20110908
Marketing Category Name
ANDA
Application Number
ANDA090182
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
1
Strength Unit
mg/mL
Pharmacy Classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-2102-2