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

"65841-836-10" National Drug Code (NDC)

Bupropion 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-10)
(Zydus Lifesciences Limited)

NDC Code65841-836-10
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-10)
Product NDC65841-836
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180802
Marketing Category NameANDA
Application NumberANDA201567
ManufacturerZydus Lifesciences Limited
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/65841-836-10





Copyright © 2007-2024 www.ndcvalidator.com