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"68788-7221-1" National Drug Code (NDC)
Bupropion Hydrochloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7221-1)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7221-1
Package Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7221-1)
Product NDC
68788-7221
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
20180726
Marketing Category Name
ANDA
Application Number
ANDA077285
Manufacturer
Preferred Pharmaceuticals 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/68788-7221-1