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"55700-257-30" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-257-30)
(Lake Erie Medical DBA Quality Care Products LLC)
NDC Code
55700-257-30
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-257-30)
Product NDC
55700-257
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
20150217
Marketing Category Name
ANDA
Application Number
ANDA077285
Manufacturer
Lake Erie Medical DBA Quality Care Products LLC
Substance Name
BUPROPION HYDROCHLORIDE
Strength
300
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/55700-257-30