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"68001-199-00" National Drug Code (NDC)
Bupropion Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (68001-199-00)
(BluePoint Laboratories)
NDC Code
68001-199-00
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (68001-199-00)
Product NDC
68001-199
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
20140207
End Marketing Date
20190731
Marketing Category Name
ANDA
Application Number
ANDA075584
Manufacturer
BluePoint Laboratories
Substance Name
BUPROPION HYDROCHLORIDE
Strength
75
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/68001-199-00