"45963-142-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (45963-142-30)
(Actavis Pharma, Inc.)

NDC Code45963-142-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (45963-142-30)
Product NDC45963-142
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20150217
Marketing Category NameANDA
Application NumberANDA077285
ManufacturerActavis Pharma, Inc.
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]

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