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"52125-332-19" National Drug Code (NDC)

Cetirizine Hydrochloride 90 TABLET in 1 VIAL (52125-332-19)
(REMEDYREPACK INC.)

NDC Code52125-332-19
Package Description90 TABLET in 1 VIAL (52125-332-19)
Product NDC52125-332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20130603
Marketing Category NameANDA
Application NumberANDA077829
ManufacturerREMEDYREPACK 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/52125-332-19





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