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"70710-1073-1" National Drug Code (NDC)
Modafinil 100 TABLET in 1 BOTTLE (70710-1073-1)
(Zydus Pharmaceuticals (USA) Inc.)
NDC Code
70710-1073-1
Package Description
100 TABLET in 1 BOTTLE (70710-1073-1)
Product NDC
70710-1073
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Modafinil
Non-Proprietary Name
Modafinil
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180104
Marketing Category Name
ANDA
Application Number
ANDA209966
Manufacturer
Zydus Pharmaceuticals (USA) Inc.
Substance Name
MODAFINIL
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC]
DEA Schedule
CIV
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-1073-1