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"52125-332-57" National Drug Code (NDC)
Cetirizine Hydrochloride 5 TABLET in 1 BOTTLE (52125-332-57)
(REMEDYREPACK INC.)
NDC Code
52125-332-57
Package Description
5 TABLET in 1 BOTTLE (52125-332-57)
Product NDC
52125-332
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20150213
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/52125-332-57