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"51660-939-13" National Drug Code (NDC)

Cetirizine Hydrochloride 120 TABLET in 1 BOTTLE (51660-939-13)
(Ohm Laboratories Inc.)

NDC Code51660-939-13
Package Description120 TABLET in 1 BOTTLE (51660-939-13)
Product NDC51660-939
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20071227
Marketing Category NameANDA
Application NumberANDA077498
ManufacturerOhm Laboratories Inc.
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-939-13





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