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"70377-034-11" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70377-034-11)
(Biocon Pharma Inc.,)
NDC Code
70377-034-11
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70377-034-11)
Product NDC
70377-034
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
20190128
Marketing Category Name
ANDA
Application Number
ANDA211020
Manufacturer
Biocon Pharma 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/70377-034-11