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"69097-877-03" National Drug Code (NDC)
Bupropion Hydrochloride (sr) 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-03)
(Cipla USA Inc.,)
NDC Code
69097-877-03
Package Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-03)
Product NDC
69097-877
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride (sr)
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20160725
Marketing Category Name
ANDA
Application Number
ANDA206674
Manufacturer
Cipla USA Inc.,
Substance Name
BUPROPION HYDROCHLORIDE
Strength
100
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/69097-877-03