NDC 0615-8581

Bupropion Hydrochloride 75 mg tablet, film coated

On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Aurobindo Pharma Limited's NDC 59651-874.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Apl Healthcare LimitedTirupati, IndiaMakes it and tests it Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections

Repackaging site

Product details

Generic drug
Bupropion: every company that makes it
Form
tablet, film coated, oral
Strength
75 mg
Approval
ANDA ANDA075491
On the market since
Apr 25, 2024
Package NDCs
0615-8581-39
Official label
DailyMed (National Library of Medicine), updated Oct 27, 2026

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