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"68788-7988-9" National Drug Code (NDC)
Bupropion Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (68788-7988-9)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7988-9
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (68788-7988-9)
Product NDC
68788-7988
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210806
Marketing Category Name
ANDA
Application Number
ANDA076143
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/68788-7988-9