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"0187-0731-07" National Drug Code (NDC)
Wellbutrin 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-07)
(Bausch Health US LLC)
NDC Code
0187-0731-07
Package Description
7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-07)
Product NDC
0187-0731
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Wellbutrin
Proprietary Name Suffix
Xl
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20030829
Marketing Category Name
NDA
Application Number
NDA021515
Manufacturer
Bausch Health US LLC
Substance Name
BUPROPION HYDROCHLORIDE
Strength
300
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/0187-0731-07