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"70677-0008-2" National Drug Code (NDC)

Fexofenadine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (70677-0008-2)
(Sunmark)

NDC Code70677-0008-2
Package Description30 TABLET, FILM COATED in 1 BOTTLE (70677-0008-2)
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

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70677-0008-2





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