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"67046-079-15" National Drug Code (NDC)
Bupropion Hydrochloride 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-079-15)
(Contract Pharmacy Services-PA)
NDC Code
67046-079-15
Package Description
15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-079-15)
Product NDC
67046-079
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20040322
Marketing Category Name
ANDA
Application Number
ANDA075932
Manufacturer
Contract Pharmacy Services-PA
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/67046-079-15