"13668-432-05" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-432-05)
(Torrent Pharmaceuticals Limited)

NDC Code13668-432-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-432-05)
Product NDC13668-432
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141031
Marketing Category NameANDA
Application NumberANDA203969
ManufacturerTorrent Pharmaceuticals Limited
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]

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