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"49999-918-30" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (49999-918-30)
(Lake Erie Medical DBA Quality Care Products LLC)
NDC Code
49999-918-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (49999-918-30)
Product NDC
49999-918
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
Lake Erie Medical DBA Quality Care Products LLC
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/49999-918-30