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"52125-556-02" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-556-02)
(REMEDYREPACK INC.)
NDC Code
52125-556-02
Package Description
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-556-02)
Product NDC
52125-556
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
20130401
Marketing Category Name
ANDA
Application Number
ANDA075932
Manufacturer
REMEDYREPACK INC.
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/52125-556-02