"70518-4049-0" National Drug Code (NDC)

Hydroxyzine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4049-0)
(REMEDYREPACK INC.)

NDC Code70518-4049-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4049-0)
Product NDC70518-4049
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydroxyzine Hydrochloride
Non-Proprietary NameHydroxyzine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240411
Marketing Category NameANDA
Application NumberANDA217652
ManufacturerREMEDYREPACK INC.
Substance NameHYDROXYZINE DIHYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAntihistamine [EPC], Histamine Receptor Antagonists [MoA]

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