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"47335-891-75" National Drug Code (NDC)
Temozolomide 20 BLISTER PACK in 1 CARTON (47335-891-75) / 1 CAPSULE in 1 BLISTER PACK
(Sun Pharmaceutical Industries, Inc.)
NDC Code
47335-891-75
Package Description
20 BLISTER PACK in 1 CARTON (47335-891-75) / 1 CAPSULE in 1 BLISTER PACK
Product NDC
47335-891
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Temozolomide
Non-Proprietary Name
Temozolomide
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20140213
Marketing Category Name
ANDA
Application Number
ANDA201742
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
TEMOZOLOMIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Alkylating Activity [MoA], Alkylating Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-891-75