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"47335-062-79" National Drug Code (NDC)

Dofetilide 4 BLISTER PACK in 1 CARTON (47335-062-79) / 10 CAPSULE in 1 BLISTER PACK (47335-062-66)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-062-79
Package Description4 BLISTER PACK in 1 CARTON (47335-062-79) / 10 CAPSULE in 1 BLISTER PACK (47335-062-66)
Product NDC47335-062
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDofetilide
Non-Proprietary NameDofetilide
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20181011
Marketing Category NameANDA
Application NumberANDA210466
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameDOFETILIDE
Strength.25
Strength Unitmg/1
Pharmacy ClassesAntiarrhythmic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-062-79





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