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"21695-137-30" National Drug Code (NDC)
Wellbutrin Xl 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-137-30)
(Rebel Distributors Corp)
NDC Code
21695-137-30
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-137-30)
Product NDC
21695-137
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Wellbutrin Xl
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20091223
Marketing Category Name
NDA
Application Number
NDA021515
Manufacturer
Rebel Distributors Corp
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/21695-137-30