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"68071-4961-2" National Drug Code (NDC)
Bupropion Hydrochloride 20 TABLET in 1 BOTTLE (68071-4961-2)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-4961-2
Package Description
20 TABLET in 1 BOTTLE (68071-4961-2)
Product NDC
68071-4961
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
NuCare 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/68071-4961-2