"68071-5214-1" National Drug Code (NDC)

Bupropion 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5214-1)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-5214-1
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5214-1)
Product NDC68071-5214
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141101
Marketing Category NameANDA
Application NumberANDA202304
ManufacturerNuCare Pharmaceuticals,Inc.
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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