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"63739-714-10" National Drug Code (NDC)

Bupropion Hydrochloride 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-714-10) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(McKesson Corporation dba SKY Packaging)

NDC Code63739-714-10
Package Description10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-714-10) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC63739-714
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
ManufacturerMcKesson Corporation dba SKY Packaging
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/63739-714-10





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