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"70677-0007-1" National Drug Code (NDC)

Fexofenadine Hydrochloride 12 TABLET, FILM COATED in 1 BLISTER PACK (70677-0007-1)
(Sunmark)

NDC Code70677-0007-1
Package Description12 TABLET, FILM COATED in 1 BLISTER PACK (70677-0007-1)
Product NDC70677-0007
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
Strength60
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70677-0007-1





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