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

"61919-136-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-136-30)
(Direct_Rx)

NDC Code61919-136-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-136-30)
Product NDC61919-136
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20170717
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerDirect_Rx
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/61919-136-30





Copyright © 2007-2024 www.ndcvalidator.com