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"80539-002-09" National Drug Code (NDC)
Cetirizine Hydrochloride (allergy) 1 BOTTLE in 1 CARTON (80539-002-09) > 30 TABLET in 1 BOTTLE
(Allwell Health Inc)
NDC Code
80539-002-09
Package Description
1 BOTTLE in 1 CARTON (80539-002-09) > 30 TABLET in 1 BOTTLE
Product NDC
80539-002
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride (allergy)
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20210215
Marketing Category Name
ANDA
Application Number
ANDA090760
Manufacturer
Allwell Health 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/80539-002-09