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"58602-877-74" National Drug Code (NDC)

Fexofenadine Hydrochloride 1 BLISTER PACK in 1 CARTON (58602-877-74) / 6 TABLET, FILM COATED in 1 BLISTER PACK
(Aurohealth LLC)

NDC Code58602-877-74
Package Description1 BLISTER PACK in 1 CARTON (58602-877-74) / 6 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC58602-877
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20231013
Marketing Category NameANDA
Application NumberANDA202039
ManufacturerAurohealth LLC
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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