NDC 33342-528

Bupropion Hydrochloride(SR) 200 mg tablet, extended release

On the label: Macleods Pharmaceuticals Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDhar, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyAug 23, 2024 · 1 inspection

Product details

Generic drug
Bupropion: every company that makes it
Form
tablet, extended release, oral
Strength
200 mg
Approval
ANDA ANDA218567
On the market since
Jun 23, 2026
Package NDCs
33342-528-09 33342-528-11
Official label
DailyMed (National Library of Medicine), updated Jun 3, 2026

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