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"23155-191-10" National Drug Code (NDC)
Bupropion Hydrochloride 1000 TABLET in 1 BOTTLE (23155-191-10)
(Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
NDC Code
23155-191-10
Package Description
1000 TABLET in 1 BOTTLE (23155-191-10)
Product NDC
23155-191
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160819
Marketing Category Name
ANDA
Application Number
ANDA206975
Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Substance Name
BUPROPION HYDROCHLORIDE
Strength
75
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/23155-191-10