"68788-7776-3" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7776-3)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7776-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7776-3)
Product NDC68788-7776
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200824
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength100
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/68788-7776-3