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"51660-939-54" National Drug Code (NDC)
Cetirizine Hydrochloride 14 TABLET in 1 BLISTER PACK (51660-939-54)
(Ohm Laboratories Inc.)
NDC Code
51660-939-54
Package Description
14 TABLET in 1 BLISTER PACK (51660-939-54)
Product NDC
51660-939
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071227
Marketing Category Name
ANDA
Application Number
ANDA077498
Manufacturer
Ohm Laboratories 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/51660-939-54