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"0781-5529-31" National Drug Code (NDC)
Bupropion Hydrochloride (xl) 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5529-31)
(Sandoz Inc.)
NDC Code
0781-5529-31
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5529-31)
Product NDC
0781-5529
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
20180108
End Marketing Date
20230531
Marketing Category Name
ANDA
Application Number
ANDA208652
Manufacturer
Sandoz Inc.
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/0781-5529-31