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"68001-261-04" National Drug Code (NDC)
Bupropion 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-261-04)
(BluePoint Laboratories)
NDC Code
68001-261-04
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-261-04)
Product NDC
68001-261
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion
Non-Proprietary Name
Bupropion
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20150122
Marketing Category Name
ANDA
Application Number
ANDA077285
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/68001-261-04