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"51655-357-26" National Drug Code (NDC)
Bupropion 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-26)
(Northwind Pharmaceuticals)
NDC Code
51655-357-26
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-26)
Product NDC
51655-357
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20200528
Marketing Category Name
ANDA
Application Number
ANDA202304
Manufacturer
Northwind Pharmaceuticals
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/51655-357-26