"49349-890-02" National Drug Code (NDC)

Fexofenadine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-890-02)
(REMEDYREPACK INC.)

NDC Code49349-890-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (49349-890-02)
Product NDC49349-890
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151026
Marketing Category NameANDA
Application NumberANDA076447
ManufacturerREMEDYREPACK INC.
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1

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