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"70518-3468-1" National Drug Code (NDC)
Cetirizine Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3468-1)
(REMEDYREPACK INC.)
NDC Code
70518-3468-1
Package Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3468-1)
Product NDC
70518-3468
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride Tablets
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220809
Marketing Category Name
ANDA
Application Number
ANDA078343
Manufacturer
REMEDYREPACK 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/70518-3468-1