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"68788-7776-3" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7776-3)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-7776-3
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7776-3)
Product NDC
68788-7776
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
20200824
Marketing Category Name
ANDA
Application Number
ANDA075932
Manufacturer
Preferred Pharmaceuticals, 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/68788-7776-3