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"50436-1570-1" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (50436-1570-1)
(Unit Dose Services)
NDC Code
50436-1570-1
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (50436-1570-1)
Product NDC
50436-1570
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20060117
Marketing Category Name
ANDA
Application Number
ANDA076143
Manufacturer
Unit Dose Services
Substance Name
BUPROPION HYDROCHLORIDE
Strength
100
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/50436-1570-1