www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"68071-5214-1" National Drug Code (NDC)
Bupropion 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5214-1)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-5214-1
Package Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5214-1)
Product NDC
68071-5214
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20141101
Marketing Category Name
ANDA
Application Number
ANDA202304
Manufacturer
NuCare Pharmaceuticals,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/68071-5214-1