"51660-939-54" National Drug Code (NDC)

Cetirizine Hydrochloride 14 TABLET in 1 BLISTER PACK (51660-939-54)
(Ohm Laboratories Inc.)

NDC Code51660-939-54
Package Description14 TABLET in 1 BLISTER PACK (51660-939-54)
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]

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