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"0185-1111-10" National Drug Code (NDC)

Bupropion Hydrochloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-1111-10)
(Eon Labs, Inc.)

NDC Code0185-1111-10
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-1111-10)
Product NDC0185-1111
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20050622
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerEon Labs, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength200
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/0185-1111-10





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