"68788-7820-6" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7820-6)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7820-6
Package Description60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7820-6)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7820-6