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"0781-5676-01" National Drug Code (NDC)
Dexmethylphenidate Hydrochloride 100 TABLET in 1 BOTTLE (0781-5676-01)
(Sandoz Inc)
NDC Code
0781-5676-01
Package Description
100 TABLET in 1 BOTTLE (0781-5676-01)
Product NDC
0781-5676
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Dexmethylphenidate Hydrochloride
Non-Proprietary Name
Dexmethylphenidate Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20150427
End Marketing Date
20191231
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA021278
Manufacturer
Sandoz Inc
Substance Name
DEXMETHYLPHENIDATE HYDROCHLORIDE
Strength
2.5
Strength Unit
mg/1
Pharmacy Classes
Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
DEA Schedule
CII
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-5676-01