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"71205-207-10" National Drug Code (NDC)
Cetirizine Hydrochloride 10 TABLET in 1 BOTTLE (71205-207-10)
(Proficient Rx LP)
NDC Code
71205-207-10
Package Description
10 TABLET in 1 BOTTLE (71205-207-10)
Product NDC
71205-207
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071227
Marketing Category Name
ANDA
Application Number
ANDA078336
Manufacturer
Proficient Rx LP
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/71205-207-10