"52125-570-21" National Drug Code (NDC)

Fexofenadine Hydrochloride 120 TABLET in 1 VIAL (52125-570-21)
(REMEDYREPACK INC.)

NDC Code52125-570-21
Package Description120 TABLET in 1 VIAL (52125-570-21)
Product NDC52125-570
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hcl
Dosage FormTABLET
UsageORAL
Start Marketing Date20130524
Marketing Category NameANDA
Application NumberANDA079112
ManufacturerREMEDYREPACK INC.
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

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