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"70518-1705-2" National Drug Code (NDC)
Cetirizine 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1705-2)
(REMEDYREPACK INC.)
NDC Code
70518-1705-2
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1705-2)
Product NDC
70518-1705
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20181203
Marketing Category Name
ANDA
Application Number
ANDA078336
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/70518-1705-2