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"63304-724-90" National Drug Code (NDC)
Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-724-90)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
63304-724-90
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-724-90)
Product NDC
63304-724
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
20210101
Marketing Category Name
ANDA
Application Number
ANDA203650
Manufacturer
Sun Pharmaceutical Industries, Inc.
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/63304-724-90