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"49349-322-02" National Drug Code (NDC)

Fexofenadine Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-322-02)
(REMEDYREPACK INC.)

NDC Code49349-322-02
Package Description30 TABLET in 1 BLISTER PACK (49349-322-02)
Product NDC49349-322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20110822
Marketing Category NameANDA
Application NumberANDA076502
ManufacturerREMEDYREPACK INC.
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength60
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/49349-322-02





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