"63629-2137-1" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2137-1)
(Bryant Ranch Prepack)

NDC Code63629-2137-1
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2137-1)
Product NDC63629-2137
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20070612
End Marketing Date20250531
Marketing Category NameANDA
Application NumberANDA077284
ManufacturerBryant Ranch Prepack
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]

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