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"46708-118-71" National Drug Code (NDC)
Bupropion Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (46708-118-71)
(Alembic Pharmaceuticals Limited)
NDC Code
46708-118-71
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (46708-118-71)
Product NDC
46708-118
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
20180618
Marketing Category Name
ANDA
Application Number
ANDA203013
Manufacturer
Alembic Pharmaceuticals Limited
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/46708-118-71