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"63187-521-30" National Drug Code (NDC)
Bupropion 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-30)
(Proficient Rx LP)
NDC Code
63187-521-30
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-30)
Product NDC
63187-521
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion
Non-Proprietary Name
Bupropion
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20140215
Marketing Category Name
ANDA
Application Number
ANDA201567
Manufacturer
Proficient Rx LP
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/63187-521-30