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"21695-017-00" National Drug Code (NDC)
Bupropion Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (21695-017-00)
(Rebel Distributors Corp.)
NDC Code
21695-017-00
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (21695-017-00)
Product NDC
21695-017
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
20000207
Marketing Category Name
ANDA
Application Number
ANDA075584
Manufacturer
Rebel Distributors Corp.
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/21695-017-00