"50090-6871-2" National Drug Code (NDC)

Bupropion Hydrochloride 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2)
(A-S Medication Solutions)

NDC Code50090-6871-2
Package Description180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2)
Product NDC50090-6871
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180420
Marketing Category NameANDA
Application NumberANDA205794
ManufacturerA-S Medication Solutions
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/50090-6871-2