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"69367-288-09" National Drug Code (NDC)
Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-09)
(Westminster Pharmaceuticals, LLC)
NDC Code
69367-288-09
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-09)
Product NDC
69367-288
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Proprietary Name Suffix
Xl
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20171001
Marketing Category Name
ANDA
Application Number
ANDA207224
Manufacturer
Westminster Pharmaceuticals, LLC
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/69367-288-09