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"37808-571-39" National Drug Code (NDC)

Allergy Relief 1 BOTTLE in 1 CARTON (37808-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE
(H E B)

NDC Code37808-571-39
Package Description1 BOTTLE in 1 CARTON (37808-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC37808-571
Product Type NameHUMAN OTC DRUG
Proprietary NameAllergy Relief
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110622
Marketing Category NameANDA
Application NumberANDA076447
ManufacturerH E B
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/37808-571-39





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