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"73581-012-02" National Drug Code (NDC)

Fexofenadine 200 TABLET in 1 BOTTLE (73581-012-02)
(YYBA Corp)

NDC Code73581-012-02
Package Description200 TABLET in 1 BOTTLE (73581-012-02)
Product NDC73581-012
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine
Non-Proprietary NameFexofenadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20260727
Marketing Category NameANDA
Application NumberANDA219032
ManufacturerYYBA Corp
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength60
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/73581-012-02





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