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"71335-0721-2" National Drug Code (NDC)

Fexofenadine Hydrochloride 15 TABLET, FILM COATED in 1 BOTTLE (71335-0721-2)
(Bryant Ranch Prepack)

NDC Code71335-0721-2
Package Description15 TABLET, FILM COATED in 1 BOTTLE (71335-0721-2)
Product NDC71335-0721
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110422
Marketing Category NameANDA
Application NumberANDA076447
ManufacturerBryant Ranch Prepack
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
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/71335-0721-2





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