"13107-067-05" National Drug Code (NDC)

Fexofenadine Hydrochloride 1 BOTTLE in 1 CARTON (13107-067-05) > 500 TABLET, FILM COATED in 1 BOTTLE
(Aurolife Pharma, LLC)

NDC Code13107-067-05
Package Description1 BOTTLE in 1 CARTON (13107-067-05) > 500 TABLET, FILM COATED in 1 BOTTLE
Product NDC13107-067
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20141119
Marketing Category NameANDA
Application NumberANDA202039
ManufacturerAurolife Pharma, LLC
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1

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