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"43826-067-03" National Drug Code (NDC)
Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43826-067-03)
(Bora Pharmaceutical Laboratories Inc.)
NDC Code
43826-067-03
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43826-067-03)
Product NDC
43826-067
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Proprietary Name Suffix
(xl)
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20180830
Marketing Category Name
ANDA
Application Number
ANDA210081
Manufacturer
Bora Pharmaceutical Laboratories 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/43826-067-03