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"70518-2335-3" National Drug Code (NDC)

Cetirizine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2335-3)
(REMEDYREPACK INC.)

NDC Code70518-2335-3
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2335-3)
Product NDC70518-2335
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191002
Marketing Category NameANDA
Application NumberANDA078336
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/70518-2335-3





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