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"67668-162-30" National Drug Code (NDC)
Cetirizine Hydrochloride 30 TABLET in 1 BOTTLE (67668-162-30)
(Unique Pharmaceutical Laboratories)
NDC Code
67668-162-30
Package Description
30 TABLET in 1 BOTTLE (67668-162-30)
Product NDC
67668-162
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
Unique Pharmaceutical Laboratories
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67668-162-30