"47335-724-66" National Drug Code (NDC)

Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride 2 BLISTER PACK in 1 CARTON (47335-724-66) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-724-66
Package Description2 BLISTER PACK in 1 CARTON (47335-724-66) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC47335-724
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180301
Marketing Category NameANDA
Application NumberANDA090818
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameFEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength60; 120
Strength Unitmg/1; mg/1
Pharmacy ClassesAdrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]

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