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"16571-402-50" National Drug Code (NDC)
Cetirizine Hydrochloride 500 TABLET in 1 BOTTLE (16571-402-50)
(Rising Pharma Holdings, Inc.)
NDC Code
16571-402-50
Package Description
500 TABLET in 1 BOTTLE (16571-402-50)
Product NDC
16571-402
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
Rising Pharma Holdings, 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/16571-402-50