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"71335-1622-1" National Drug Code (NDC)
Bupropion 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1622-1)
(Bryant Ranch Prepack)
NDC Code
71335-1622-1
Package Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1622-1)
Product NDC
71335-1622
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20141101
Marketing Category Name
ANDA
Application Number
ANDA202304
Manufacturer
Bryant Ranch Prepack
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/71335-1622-1