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"70518-1989-0" National Drug Code (NDC)

Cetirizine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1989-0)
(REMEDYREPACK INC.)

NDC Code70518-1989-0
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1989-0)
Product NDC70518-1989
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190327
Marketing Category NameANDA
Application NumberANDA078317
ManufacturerREMEDYREPACK INC.
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1989-0





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