"62756-064-59" National Drug Code (NDC)

Fingolimod 1 BLISTER PACK in 1 CARTON (62756-064-59) / 7 CAPSULE in 1 BLISTER PACK
(Sun Pharmaceutical Industries, Inc.)

NDC Code62756-064-59
Package Description1 BLISTER PACK in 1 CARTON (62756-064-59) / 7 CAPSULE in 1 BLISTER PACK
Product NDC62756-064
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFingolimod
Non-Proprietary NameFingolimod
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20221025
Marketing Category NameANDA
Application NumberANDA208014
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameFINGOLIMOD HYDROCHLORIDE
Strength.5
Strength Unitmg/1
Pharmacy ClassesSphingosine 1-Phosphate Receptor Modulators [MoA], Sphingosine 1-phosphate Receptor Modulator [EPC]

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