"68788-7820-1" National Drug Code (NDC)

Bupropion Hydrochloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7820-1)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7820-1
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7820-1)
Product NDC68788-7820
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20201113
Marketing Category NameANDA
Application NumberANDA077284
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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