"52125-332-08" National Drug Code (NDC)

Cetirizine Hydrochloride 10 TABLET in 1 BOTTLE (52125-332-08)
(REMEDYREPACK INC.)

NDC Code52125-332-08
Package Description10 TABLET in 1 BOTTLE (52125-332-08)
Product NDC52125-332
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20150327
Marketing Category NameANDA
Application NumberANDA077829
ManufacturerREMEDYREPACK INC.
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1

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