"68788-8922-6" National Drug Code (NDC)

Bupropion Hydrochloride 160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8922-6)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-8922-6
Package Description160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8922-6)
Product NDC68788-8922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20150922
Marketing Category NameANDA
Application NumberANDA078866
ManufacturerPreferred 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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