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"61919-536-30" National Drug Code (NDC)

Fexofenadine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (61919-536-30)
(DirectRX)

NDC Code61919-536-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-536-30)
Product NDC61919-536
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151203
Marketing Category NameANDA
Application NumberANDA076447
ManufacturerDirectRX
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/61919-536-30





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