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"0615-8505-39" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8505-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)
NDC Code
0615-8505-39
Package Description
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8505-39)
Product NDC
0615-8505
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20220801
Marketing Category Name
ANDA
Application Number
ANDA211020
Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs
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/0615-8505-39