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"0093-0739-05" National Drug Code (NDC)
Donepezil Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (0093-0739-05)
(Teva Pharmaceuticals USA Inc)
NDC Code
0093-0739-05
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (0093-0739-05)
Product NDC
0093-0739
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Donepezil Hydrochloride
Non-Proprietary Name
Donepezil Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110531
End Marketing Date
20150731
Marketing Category Name
ANDA
Application Number
ANDA090425
Manufacturer
Teva Pharmaceuticals USA Inc
Substance Name
DONEPEZIL HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0739-05