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"0093-5502-01" National Drug Code (NDC)

Budeprion 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0093-5502-01)
(TEVA Pharmaceuticals USA Inc)

NDC Code0093-5502-01
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0093-5502-01)
Product NDC0093-5502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBudeprion
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20040323
End Marketing Date20150131
Marketing Category NameANDA
Application NumberANDA075913
ManufacturerTEVA Pharmaceuticals USA Inc
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/0093-5502-01





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