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"68001-519-05" National Drug Code (NDC)
Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-519-05)
(BluePoint Laboratories)
NDC Code
68001-519-05
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-519-05)
Product NDC
68001-519
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
20211213
Marketing Category Name
ANDA
Application Number
ANDA210497
Manufacturer
BluePoint Laboratories
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/68001-519-05