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"0185-0415-60" National Drug Code (NDC)
Bupropion Hydrochloride 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0415-60)
(Eon Labs, Inc.)
NDC Code
0185-0415-60
Package Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0415-60)
Product NDC
0185-0415
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20040322
End Marketing Date
20250731
Marketing Category Name
ANDA
Application Number
ANDA075932
Manufacturer
Eon Labs, Inc.
Substance Name
BUPROPION HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0185-0415-60