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"70518-0182-1" National Drug Code (NDC)
Cetirizine Hydrochloride 30 TABLET in 1 BOTTLE, PLASTIC (70518-0182-1)
(REMEDYREPACK INC.)
NDC Code
70518-0182-1
Package Description
30 TABLET in 1 BOTTLE, PLASTIC (70518-0182-1)
Product NDC
70518-0182
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170127
Marketing Category Name
ANDA
Application Number
ANDA077829
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/70518-0182-1