"71335-1217-4" National Drug Code (NDC)

Fexofenadine Hcl 90 TABLET in 1 BOTTLE (71335-1217-4)
(Bryant Ranch Prepack)

NDC Code71335-1217-4
Package Description90 TABLET in 1 BOTTLE (71335-1217-4)
Product NDC71335-1217
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hcl
Non-Proprietary NameFexofenadine Hcl
Dosage FormTABLET
UsageORAL
Start Marketing Date20160819
Marketing Category NameANDA
Application NumberANDA204097
ManufacturerBryant Ranch Prepack
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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