"70677-0008-1" National Drug Code (NDC)

Fexofenadine Hydrochloride 15 TABLET, FILM COATED in 1 BLISTER PACK (70677-0008-1)
(Sunmark)

NDC Code70677-0008-1
Package Description15 TABLET, FILM COATED in 1 BLISTER PACK (70677-0008-1)
Product NDC70677-0008
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20161012
Marketing Category NameANDA
Application NumberANDA202039
ManufacturerSunmark
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1

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