www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"0781-1064-31" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (0781-1064-31)
(Sandoz Inc)

NDC Code0781-1064-31
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0781-1064-31)
Product NDC0781-1064
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20000207
End Marketing Date20211130
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerSandoz 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/0781-1064-31





Copyright © 2007-2024 www.ndcvalidator.com