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"72189-305-30" National Drug Code (NDC)

Fexofenadine 30 TABLET in 1 BOTTLE (72189-305-30)
(DirectRx)

NDC Code72189-305-30
Package Description30 TABLET in 1 BOTTLE (72189-305-30)
Product NDC72189-305
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine
Non-Proprietary NameFexofenadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20211217
End Marketing Date20230720
Marketing Category NameANDA
Application NumberANDA204097
ManufacturerDirectRx
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72189-305-30





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