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"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 Code
62756-064-59
Package Description
1 BLISTER PACK in 1 CARTON (62756-064-59) / 7 CAPSULE in 1 BLISTER PACK
Product NDC
62756-064
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fingolimod
Non-Proprietary Name
Fingolimod
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20221025
Marketing Category Name
ANDA
Application Number
ANDA208014
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
FINGOLIMOD HYDROCHLORIDE
Strength
.5
Strength Unit
mg/1
Pharmacy Classes
Sphingosine 1-Phosphate Receptor Modulators [MoA], Sphingosine 1-phosphate Receptor Modulator [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/62756-064-59