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"69452-465-81" National Drug Code (NDC)
Cetirizine Hydrochloride 400 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-465-81)
(Bionpharma Inc.)
NDC Code
69452-465-81
Package Description
400 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-465-81)
Product NDC
69452-465
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20241020
Marketing Category Name
ANDA
Application Number
ANDA078862
Manufacturer
Bionpharma 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/69452-465-81