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"72189-134-60" National Drug Code (NDC)
Bupropion Hydrochloride 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-60)
(DIRECT RX)
NDC Code
72189-134-60
Package Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-60)
Product NDC
72189-134
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
20201015
Marketing Category Name
ANDA
Application Number
ANDA210497
Manufacturer
DIRECT RX
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/72189-134-60