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"0527-2430-32" National Drug Code (NDC)
Bupropion Hydrochloride (xl) 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2430-32)
(Lannett Company Inc.)
NDC Code
0527-2430-32
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2430-32)
Product NDC
0527-2430
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride (xl)
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20180108
Marketing Category Name
ANDA
Application Number
ANDA208652
Manufacturer
Lannett Company Inc.
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/0527-2430-32