www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"76519-1021-5" National Drug Code (NDC)
Bupropion Hydrochloride 150 TABLET, EXTENDED RELEASE in 1 CONTAINER (76519-1021-5)
(H.J. Harkins Company Inc.)
NDC Code
76519-1021-5
Package Description
150 TABLET, EXTENDED RELEASE in 1 CONTAINER (76519-1021-5)
Product NDC
76519-1021
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20170103
Marketing Category Name
ANDA
Application Number
ANDA206556
Manufacturer
H.J. Harkins Company Inc.
Substance Name
BUPROPION HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Aminoketone [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/76519-1021-5