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"49349-230-02" National Drug Code (NDC)
Bupropion Hydrocloride 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-230-02)
(REMEDYREPACK INC.)
NDC Code
49349-230-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (49349-230-02)
Product NDC
49349-230
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrocloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110314
Marketing Category Name
ANDA
Application Number
ANDA075584
Manufacturer
REMEDYREPACK INC.
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/49349-230-02