"16571-402-50" National Drug Code (NDC)

Cetirizine Hydrochloride 500 TABLET in 1 BOTTLE (16571-402-50)
(Rising Pharma Holdings, Inc.)

NDC Code16571-402-50
Package Description500 TABLET in 1 BOTTLE (16571-402-50)
Product NDC16571-402
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20091001
Marketing Category NameANDA
Application NumberANDA077829
ManufacturerRising Pharma Holdings, Inc.
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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