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"71610-131-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-131-30)
(Aphena Pharma Solutions - Tennessee, LLC)

NDC Code71610-131-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-131-30)
Product NDC71610-131
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140624
Marketing Category NameANDA
Application NumberANDA077285
ManufacturerAphena Pharma Solutions - Tennessee, LLC
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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/71610-131-30





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