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"76420-812-01" National Drug Code (NDC)
Bupropion Hydrochloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-01)
(Asclemed USA, Inc.)
NDC Code
76420-812-01
Package Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-01)
Product NDC
76420-812
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
20150217
Marketing Category Name
ANDA
Application Number
ANDA077285
Manufacturer
Asclemed USA, Inc.
Substance Name
BUPROPION HYDROCHLORIDE
Strength
300
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/76420-812-01