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"49349-890-50" National Drug Code (NDC)

Fexofenadine Hydrochloride 40 TABLET, FILM COATED in 1 BOTTLE (49349-890-50)
(REMEDYREPACK INC.)

NDC Code49349-890-50
Package Description40 TABLET, FILM COATED in 1 BOTTLE (49349-890-50)
Product NDC49349-890
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131204
Marketing Category NameANDA
Application NumberANDA076447
ManufacturerREMEDYREPACK INC.
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/49349-890-50





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