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"67046-079-21" National Drug Code (NDC)

Bupropion Hydrochloride 21 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-079-21)
(Contract Pharmacy Services-PA)

NDC Code67046-079-21
Package Description21 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-079-21)
Product NDC67046-079
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20040322
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerContract Pharmacy Services-PA
Substance NameBUPROPION HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesAminoketone [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/67046-079-21





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