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"10202-939-14" National Drug Code (NDC)
Cetirizine Hydrochloride 14 TABLET in 1 BLISTER PACK (10202-939-14)
(7-ELEVEN)
NDC Code
10202-939-14
Package Description
14 TABLET in 1 BLISTER PACK (10202-939-14)
Product NDC
10202-939
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190731
Marketing Category Name
ANDA
Application Number
ANDA077498
Manufacturer
7-ELEVEN
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/10202-939-14