"70518-3789-0" National Drug Code (NDC)

Fexofenadine Hcl 30 TABLET in 1 BOTTLE, PLASTIC (70518-3789-0)
(REMEDYREPACK INC.)

NDC Code70518-3789-0
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70518-3789-0)
Product NDC70518-3789
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hcl
Non-Proprietary NameFexofenadine Hcl
Dosage FormTABLET
UsageORAL
Start Marketing Date20230713
Marketing Category NameANDA
Application NumberANDA204097
ManufacturerREMEDYREPACK INC.
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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