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"51655-194-52" National Drug Code (NDC)
Cetirizine 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-52)
(Northwind Pharmaceuticals, LLC)
NDC Code
51655-194-52
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-52)
Product NDC
51655-194
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20221018
Marketing Category Name
ANDA
Application Number
ANDA078336
Manufacturer
Northwind Pharmaceuticals, LLC
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/51655-194-52