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"52817-346-30" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-346-30)
(TruPharma LLC)
NDC Code
52817-346-30
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52817-346-30)
Product NDC
52817-346
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Proprietary Name Suffix
Xl
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20220127
Marketing Category Name
ANDA
Application Number
ANDA211200
Manufacturer
TruPharma 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/52817-346-30