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"69680-157-92" National Drug Code (NDC)
Bupropion Hydrochloride (xl) 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-92)
(Vitruvias Therapeutics)
NDC Code
69680-157-92
Package Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-92)
Product NDC
69680-157
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
20230417
Marketing Category Name
ANDA
Application Number
ANDA208652
Manufacturer
Vitruvias Therapeutics
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/69680-157-92